#Next-Generation Sequencing
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Maximizing Efficiency: Best Practices for Using Sequencing Consumables
By implementing these best practices, researchers can streamline sequencing workflows, increase throughput, and achieve more consistent and reproducible results in genetic research. Sequencing Consumables play a crucial role in genetic research, facilitating the preparation, sequencing, and analysis of DNA samples. To achieve optimal results and maximize efficiency in sequencing workflows, it's essential to implement best practices for using these consumables effectively.
Proper planning and organization are essential for maximizing efficiency when using Sequencing Consumables. Before starting a sequencing experiment, take the time to carefully plan out the workflow, including sample preparation, library construction, sequencing runs, and data analysis. Ensure that all necessary consumables, reagents, and equipment are readily available and properly labeled to minimize disruptions and delays during the experiment.
Optimizing sample preparation workflows is critical for maximizing efficiency in sequencing experiments. When working with Sequencing Consumables for sample preparation, follow manufacturer protocols and recommendations closely to ensure consistent and reproducible results. Use high-quality consumables and reagents, and perform regular quality control checks to monitor the performance of the workflow and identify any potential issues early on.
Utilizing automation technologies can significantly increase efficiency when working with Sequencing Consumables. Automated sample preparation systems and liquid handling robots can streamline repetitive tasks, reduce human error, and increase throughput. By automating sample processing and library construction workflows, researchers can save time and resources while improving consistency and reproducibility in sequencing experiments.
Get More Insights On This Topic: Sequencing Consumables
#Sequencing Consumables#DNA Sequencing#Laboratory Supplies#Genetic Analysis#Next-Generation Sequencing#Molecular Biology#Research Tools#Bioinformatics
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#NSCLC#HER2#KRAS#MET#copy-number gains#oncogene overlap#tissue-based NGS#mutational landscape#genomic profiling#precision oncology#survival impact#lung cancer research#targeted therapies#cancer genomics#molecular oncology#personalized medicine#cancer heterogeneity#next-generation sequencing#tumor behavior#therapeutic strategies.#Youtube
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Clinical Oncology Next Generation Sequencing Market - Forecast(2024 - 2030)
Clinical Oncology Next Generation Sequencing Market Overview
Clinical Oncology Next Generation Sequencing Market size was valued at $1.4 billion in 2020 and projected to grow at a CAGR of 13.6% during the forecast period 2021-2026. Next-generation sequencing is a technique that helps to simultaneously perform multiple reactions from which it is possible to sequence DNA or RNA. Biological sciences have been revolutionized by massively parallel sequencing technologies i.e. next-generation sequencing (NGS). Targeted sequencing and re-sequencing provides advantages such as high throughput and lower cost per sample of the process thereby enhancing its application Companion Diagnostics. It is a method of assessing the nucleotide sequence in a DNA section and is used for oncology research and enables researchers to carry out a wide range of applications and study biological systems with their ultra-high throughput, scalability, and speed at a level never before possible. In addition, sequencing of the next generation helps in the evaluation of several genes in a single assay, thus reducing the need to order numerous tests to evaluate the underlying mutation thereby driving the Clinical Oncology Next Generation Sequencing Market. In tumour science, a high implementation rate in whole-genome sequencing (WGS) has been seen in recent years driving the Clinical Oncology Next Generation Sequencing Market Industry. The emergence of next-generation sequencing clinical applications in precision oncology has accelerated key company’s efforts to create new platforms that can be used for genomic assays. In February 2021, for instance, Congenica partnered with Gabriel Precision Oncology Ltd. to create an automatic software interface for clinical oncology interpretation using biotechnology. In routine clinical practice, this product will promote NGS-based molecular diagnostics of tumours.
Report Coverage
The report: “Clinical Oncology Next Generation Sequencing Market Forecast (2021-2026)”, by Industry ARC, covers an in-depth analysis of the following segments of the Clinical Oncology Next Generation Sequencing Market.
By Technology Type: Whole Genome Sequencing, Whole Exome Sequencing and Targeted Sequencing & Resequencing Centrifuges.
By Application: Screening - Sporadic Cancer and Inherited Cancer, Companion Diagnostics and Other Diagnostics.
By Workflow: NGS Pre-Sequencing, NGS Sequencing and NGS Data Analysis.
By End Use: Hospitals/Clinics, Laboratories and Research Labs.
By Geography: North America (U.S, Canada and Mexico), Europe (Germany, UK, France, Italy, Spain, Russia and Rest of Europe), Asia Pacific (China, Japan India, South Korea, Australia & New Zealand, and Rest of Asia Pacific), South America (Brazil, Argentina and Rest of South America) and RoW (Middle East and Africa).
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Key Takeaways
The increasing need for successful treatment of various cancer types and scientific developments in immunology, molecular biology and genetics are likely to contribute to the growth of the Clinical Oncology Next Generation Sequencing industry.
Geographically, North America Clinical Oncology Next Generation Sequencing Market held the largest revenue share of 36% in 2020 owing to an increased emphasis on cancer treatment by government agencies, a rise in healthcare spending and the presence of sufficient resources in the healthcare industry in this region.
The growth of the market is driven by rising research and development activities using NGS technologies, growing NGS applications in clinical diagnosis and discovery applications that demand NGS technology.
Detailed analysis on the Strength, Weakness and Opportunities of the prominent players operating in the market is provided in the Clinical Oncology Next Generation Sequencing Market.
Clinical Oncology Next Generation Sequencing Market Segment Analysis - By Technology Type
Based on Technology Type, Clinical Oncology Next Generation Sequencing Market is segmented into Whole Genome Sequencing, Whole Exome Sequencing and Targeted Sequencing & Resequencing Centrifuges. Targeted Sequencing & Resequencing Centrifuges accounted for the largest revenue market share in 2020 help reduce the expense, time, and volume of data analysed during tumour sample sequencing which is anticipated to favourably impact the segment growth. Targeted sequencing uses deep sequencing within an area of interest to identify recognized and novel variants. Illumina's 523-gene panel contains all the probable genes that have the ability to cause malignant tumours to develop. Medical laboratories have introduced the product to diagnose patients suffering from acute myeloid leukaemia. In addition, the efficacy of targeted panels for the identification of malignant tumors improves their clinical usefulness. In 64% of cancer cases, NGS panels are clinically beneficial, according to a report reported in JCO Precision Oncology, 2020 driving the Clinical Oncology Next Generation Sequencing Industry. Whole Genome Sequencing segment is anticipated to grow with the fastest CAGR of 8.3% in the forecast period 2021-2026 owing to the usefulness of this technology to discern and compare normal tissues from tumour tissues, segment growth. Moreover, whole-genome sequencing of cancer patients helps to identify therapies for existing mutations and also helps to target mutations ahead of time. It also helps analyse the prognosis of cancer and establish a treatment regimen depending on the genes affected aiding to the Clinical Oncology Next Generation Sequencing Market growth.
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Clinical Oncology Next Generation Sequencing Market Segment Analysis - By Application
Based on Application, Clinical Oncology Next Generation Sequencing Market is segmented into Screening - Sporadic Cancer and Inherited Cancer, Companion Diagnostics and Other Diagnostics. Screening accounted for the largest revenue market share in 2020. The most effective way to identify genetic alterations that can be targeted for clinical benefit in cancer patients is currently considered to be NGS-based testing. This technology enables clinicians to analyse several alterations of genes simultaneously. Moreover, as opposed to other pathology methods, technology needs less tumor tissues. An increase in the number of cancer sequencing projects is also increasing the growth of the segment. For instance, 38 different types of cancer were analysed by the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium by sequencing more than 2,600 tumour samples aiding to the market's growth. Companion Diagnostics segment is anticipated to grow with the fastest CAGR of 9.1% during the forecast period 2021-2026. Efforts taken by key market participants to develop advanced computational tools propel the segment growth. For instance, in January 2021, scientists from the MD Anderson Cancer Center created CopyKAT, a new computational tool to distinguish between normal as well as cancer cells in a tumour thus enhancing the Companion Diagnostics segment demand.
Clinical Oncology Next Generation Sequencing Market Segment Analysis - By Geography
Based on Geography, North America Clinical Oncology Next Generation Sequencing Market accounted for the 36% revenue share in 2020. This rise is accounted for by substantial efforts made by regulatory bodies to boost cancer screening detection in the U.S. For instance, the U.S.-initiated Cancer Genome Atlas programme, Next-generation sequencing has been conducted by the National Cancer Institute (NCI) of more than 20,000 primary cancer samples from 33 different cancer types. A consortium of 12 cancer centres, including Johns Hopkins University, Dana-Farber Cancer Institute, and others throughout the United States, is the NCI's Cancer Aim Discovery and Growth Network enhancing the Clinical Oncology Next Generation Sequencing Market. In January 2020, in the United States, the Intelligence Advanced Research Projects Activity provided $23 million to the Broad Institute and Harvard University, and DNA Script. In addition, the emergence of a range of laboratories, academic institutions and hospitals that provide early cancer detection and treatment services based on NGS is owing to the growth of the regional sector. For instance, EasyDNA Canada, a Toronto-based DNA Biotechnology testing company, provides Cancer Predisposition Panel tests that use NGS technology to recognise mutations in a total of 98 genes associated with 25 inherited cancers. The test helps to recognise people who at a later stage of their lives are at a high risk of developing cancer drive the regional growth. Asia-Pacific is predicted to be the fastest-growing region during the forecast period 2021- 2026 owing to the increasing automation in the pre-sequencing protocols in this particular region thereby aiding to regional growth.
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Clinical Oncology Next Generation Sequencing Market Drivers
Increasing Prevalence of Cancer:
Cancer is the second leading cause of death worldwide, according to the WHO, and was responsible for an estimated 9.6 million fatalities in 2018. Need for cancer therapies is rising with the increasing number of cancer cases and deaths caused by cancer. Thus government of various economies focus on drug development, targeted sequencing for the reduction of cancer cases have also increased. Rising biomedical research using next-generation clinical oncology sequencing is estimated to create a favourable environment in the near future for the growth of the next-generation clinical oncology sequencing industry. With substantial advances in genetic sequencing and biomedical science, much research into monoclonal antibodies is now focused on discovering new development targets and optimizing their effectiveness for clinical practice, demonstrating a significant effect on the need for the Clinical Oncology Next Generation Sequencing Market.
Decreasing Sequencing Costs Are Highly Likely To Lead To Market Growth:
In clinical oncology, research and academic institutions are generally interested in the characteristic features of next-generation targeted sequencing technology. The next-generation sequencing techniques in clinical oncology give a high percentage of reads and cost-effectiveness per read. The arrival of low-cost sequencing platforms on the market has made this possible. This increases the overall growth of the next-generation sequencing market for clinical oncology. Several industry players, such as Roche and Illumina, have launched sequencing techniques that have reduced the cost of next-generation sequencing for clinical oncology. Government support for life science research is also estimated to result in the availability of funding for the undertaking of different next-generation sequencing projects in clinical oncology, as well as for the jobs of the staff needed which further act as a driving factor for the growth of the Clinical Oncology Industry.
Clinical Oncology Next Generation Sequencing Market Challenges
Major Regulatory Concerns & Lack Skilled Professionals:
Regulatory concerns regarding usage of Clinical Oncology Next Generation Sequencing Analysis and growing stringent government policy and regulation towards the quantity of service being used in application is restraining growth of the market. Market restrain is also owing to the difficulty in the management of large data and complications, associated with Big Data management. In addition, some of the ethical issues associated with whole-genome sequencing, coupled with the lack of awareness among people are constraining the growth of the market. In addition, the lack of skilled professionals with the sequencing that could be serious for diagnosis purpose set to restrain the market growth. It gets difficult when in an emergency situation, the queue of patients have to wait for experts in the required field negatively impacting the growth.
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Clinical Oncology Next Generation Sequencing Industry Outlook:
Product launches, mergers and acquisitions, joint ventures and geographical expansions are key strategies adopted by players in the Clinical Oncology Next Generation Sequencing Market. Clinical Oncology Next Generation Sequencing Market top 10 companies are Illumina, Inc., Qiagen N.V., Pacific Biosciences of California, Inc., Takara Bio, Inc., Creative Biolabs, Mogene LC, F. Hoffmann-La Roche Ltd, Oxford Nanopore Technologies, Agilent Technologies and Thermo Fisher Scientific Inc.
Acquisitions/Product Launches:
In January 2021, 4baseCare, a start-up in precision oncology, partnered with the Advanced Centre for Cancer Treatment, Study and Education (ACTREC), India, to develop ClinOme, an AI-driven platform for clinical interpretation
In May 2020, Illumina, Inc., has partnered with Burning Rock Biotech Limited, a cancer test provider based in China, to promote the standardisation and development within China of the selection of NGS-based cancer therapy. The company has also signed an agreement to develop and commercialise myChoice tumour testing in China with Myriad Genetics, Inc.
In March 2019, Oxford Nanopore Technologies launched a new paradigm of smaller, on-demand DNA or RNA sequencing tests with the potential to transform a variety of applications where rapid insights are needed at a low cost.
#Clinical Oncology Next Generation Sequencing Market#Clinical Oncology Next Generation Sequencing Market Size#Sporadic Cancer#Clinical Oncology Next Generation Sequencing Market Share#Clinical Oncology Next Generation Sequencing Market Analysis#next-generation sequencing#Resequencing Centrifuges Clinical Oncology Next Generation Sequencing Market Revenue#Clinical Oncology Next Generation Sequencing Market Trends#Clinical Oncology Next Generation Sequencing Market Growth#Clinical Oncology Next Generation Sequencing Market Research#Clinical Oncology Next Generation Sequencing Market Outlook#Clinical Oncology Next Generation Sequencing Market Forecast
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Biotech Breakthroughs: Cutting-Edge Innovations That Will Change Health Care
Introduction
The field of biotechnology is at the forefront of some of the most groundbreaking advancements in healthcare. With new discoveries and innovations emerging at an unprecedented rate, biotech is poised to transform the way we approach health care. From revolutionary treatments to personalized medicine, the potential of biotech to improve lives is immense. In this article, we’ll delve into the most significant biotech breakthroughs and how they are set to change health care as we know it. Read to continue
#Tech Trends#Tagsadvanced drug development#AI in drug development#biopharmaceuticals#biotech breakthroughs#biotech in diagnostics#cancer immunotherapy#cutting-edge innovations in health care#digital therapeutics#gene editing CRISPR-Cas9#liquid biopsies#neurotechnology#next-generation sequencing#personalized medicine#point-of-care testing#psychobiotics#regenerative medicine#stem cell therapy#tissue engineering#Technology#Science#business tech#Adobe cloud#Trends#Nvidia Drive#Analysis#Tech news#Science updates#Digital advancements#Tech trends
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Sequencing: A Deep Dive into the History of DNA Techniques
Sequencing: A Deep Dive into the History of DNA Techniques The evolution of DNA sequencing technologies marks a fascinating journey of scientific breakthroughs, from the early days of manual, labor-intensive methods to the current era of high-throughput, automated systems. This history can be divided into three main generational shifts, each characterized by significant advancements in…
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#DNA Sequencing#DNA Sequencing Evolution#Next-Generation Sequencing#Sequencing Technology Milestones
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Tekmatic: Next-Generation Sequencing | Explore the Technology
Next-generation sequencing (NGS) describes high-throughput methods that can swiftly determine the sequence of a specific nucleic acid strand, such as DNA or RNA. How we perform genomics research has altered as a result of these tools. There are numerous methods that use different operating principles under the umbrella term "next-generation sequencing."
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THIS THING IS SCUUUFFED AS HELL & ITS ALSO THE BEST THING I HAVE ANIMATED THUS FAR. IM SO IN LOVE WITH EMIZEL. JUST WISH I GAVE HIM MORE STUPID TATTOOS. NEXT TIME THO. NEXT TIME. I ALSO LOVE VEX&VIV SOOOO MUCH. charlies flavor of Deranged is my FAVORITE!!
#cw gore#jrwi fanart#jrwi show#jrwi suckening#jrwi suckening spoilers#ACTULY FINISHED THIS A WHILE AGO. kept going back n forth between trying to work on it more or call it done#in the end i chose DONE!! i worked on this for a full day n a half. NO idea what possesed me but it is NOT happenin again anytime soon#i shall do better NEXT TIME!! in the meantime tho OH MY GOOOOOD WHO WANTS TO SCREAM ABT THE SUCKENING WITH ME#THE FUCKINNN THE FUCKIN THING WITH VEX N VIV BEING THE SHADOW LEADERS OF THE FANGS/DEMONS#OH MMYY GOOOODDD THATS THEIR LIL MEAT GENERATOR... THTS SO FUCKED UP AND COOL UUUGHHH I LOVE THEM...#THEIR FLAVORE IS SO WONDERFUL. I LOOOVE HOW SILLY THEY ARE. MAKING PUNS WHILE PULLIN A SCREAMING VICTIM APART#vex n his lil fashiony art workshop and viv n her sterile n clean doctors office#i bet she doesnt even HAVE a medical liscense. it would be funny if vex did tho. could u imagine#they main MEDIC in tf2 together. viv is the battlemedic while vex only pocket medics for her. COULD U IMAGINE#guh i could go on abt these two forever n ever n ever i LOVE THEMM i gotta draw em more....#OH ALSO before i run outa room. i should say. i took inspiration from a tf2 animation called POOTIS ENGAGED#the animator. Ceno0. uses black bars in the action sequences in SUCH A COOL WAYYY everytime i watch that video i feel inspired#oneday ill make more complex fight scenes... one day....#in the meantime UGHHH I LOVE THE SUCKENING SO MUUUCH CAN I JUST FUCKIN SAAAYY THAT I THINK EMIZEL IS A SMART COOKIE!!#THESE PPL FUCKING FEAR HIM NOW!!! 'SHAMIA SHAMI' IS NOW THEIR MORTAL ENEMY!! POWERFUL ILLUSIONIST. CANT DIE.#THAT PART AT THE END THERE WHERE HE FUCKIN. KILLS HIMSELF INFRONTA THEM. THATS SO AWESOME. THATS SO METAL. AND THEN HE COMES BACK!!#I WATCHED EP 7 ASWELL BUT I WONT SPOIL IT HERE. BUT OMYGOD. EMIZEL IS SO COOL AND CAPABLE N SMART N FUNNY N UGHHHHHH I LOVE HIMMMMM#OKAY THATS MY RAMBLE FOR THE DAY THANKYOU FOR READING. I READ ALL TAGS SO YOU SHOULD RAMBLE TOO. IF YOU WANT. IF YOU CAN.
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THOAM ISSUE 7 PAGE 32
NEXT PAGE –> <– PREVIOUS PAGE
ISSUE 1 - ISSUE 2 - ISSUE 3 - ISSUE 4 - ISSUE 5 - ISSUE 6
#thoam#issue 7#shadow the hedgehog#sonic the hedgehog#sonic the werehog#dark shadow#im sooo proud of this one and the next one#but the whole sequence in general#i really outdid myself with the layouts and everything here
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a friend who'd wait :)
#im posting this very late because i was sort of weary of how it came out and ended up messing w it until it was like 4am oops.#and i have plans tmrw so... oh well! i did my best and ill put it out while i can!#and i tried to make the scene match barnard's colors lol#finn's ocs#finn's art#i know i said id do more sillay stuff with the simpler screentone only style but i had a couple more of these in me#and this is the first piece im making thats like an actual part of the story too rather than just setting stuff for fun#i wanna write something to go with it too but for now ill just sort of briefly explain the context in the tags here:#barnard has a pretty bad case of OCD and his compulsions have made it difficult to make friends in the past#he was never outright bullied or anything but people just didnt really have the patience to deal with it#he has compulsions that include stuff like walking through doors until it feels right and needing things to be perfectly aligned#which in group settings has lead to people having to wait for him to finish his rituals and join them#they might find it tolerable at first but eventually they grow impatient and hes just... not invited to stuff anymore#but juno is a newer member of the guild who ends up frequenting the same library. hes also kinda a little weird#and they dont become fast friends or anything but just sort of naturally spend time in the same place#though they never plan meetups they eventually fall into a routine. around the same time theyd just both be at the library#and read next to each other. and maybe talk a bit. and eventually they end up walking back to the guildhall together#since theyre going to the same place after all. and juno always waits for barnard outside the door#eventually barnard asks if this bothers him. juno kinda just tells him 'of course it does' without any malice or anything. just a statement#barnard is surprised and apologizes and juno says not to. but the next day juno doesnt show up at the usual time.#barnard assumes hes committed somekinda more by bringing it up. he ends up staying there late reading to get his mind off it & not ruminate#but when he leaves juno is in fact still waiting for him down the hall (see pic) having collected a bunch of books literally abt ocd#he fell asleep bc barnard stayed later than expected. and hes an eepy guy generally. and also one very bad at expressing himself#but now barnard gets that juno's 'of course it [bothers me]' had the implication of 'but its worth it' which no friend has previously done.#and from the interaction juno was also able to understand that this isn't something barnard just does for the hell of it so. he studies.#and checks a bunch of stuff out because he thinks it could help his friend too (theres ocd workbooks and such- i remember working w them)#and thats the point where they became more ''friends'' than ''pleasant library acquaintances''#from there on they also do get into juno's problems. whole other bag of worms. but this specific scene is more about bernard from his pov#sorry about when i said briefly explain. i lied </3#but compared to the whole sequence im picturing its brief so shhh
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we need to make using chatgpt embarrassing. what do you mean you don't care if what you write is full of nonsense presented as facts
#chatgpt#ai#“ai” is just aggregating historical data to predict the next output in a sequence which is why is can output complete nonsense as fact#generative ai
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I'VE FINALLY FINISHED BROTHERSHIP IT WAS SOOOOO GOOD!!!!!!!
#clai speaks#spoilers in the tags probably#ahhh first of all i am still astounded the game exists at all. we all thought m&l was done forever but here it is!!!#the timing of me playing superstar saga and getting really into mario last year couldnt have been better#i mean i probably would have played brothership still even if mario hadnt become a main interest of mine like that. but anyway#absolutely stellar re-entry into the series it did not disappoint in the SLIGHTEST#i think i 100%'d it? only thing i didnt do was finish that last dyode dance sequence but like its fiiiine#took about 50 hours i didnt get a chance to check my final time. really surprised that the game went that long!#i dont think it was a bad thing at all though. the game mostly didnt feel like it was overstaying its welcome#i did think lottacoins and the lower level solitree went a tad too long and i didnt like them but only a little. they're still fine sections#surprised that i didnt even feel like the sidequests were a drag they were all alright!#character interactions were so good ofc. love the new cast!! starlow felt a bit flat which is a shame but she also didnt appear much so#the sidequest where she visits bowser and he calls her chippy!!!! made me so happy!!!!!#all the callbacks were so good i'm glad they can still do that. yelled out loud after finding the peasley reef#docking points for no dreambert reef however. jail worthy offence#on reclusa specifically i dont have a lot to say about his character he's just your typical evil for the sake of evil villain#but i have to say i Love his design. the really exaggerated facial expressions and that clown neck frill. really fun character actually!!#ahhh call me childish but i'm never a fan of endings where friends separate but i like to think the second uni-tree--#--will allow them to link back up once its grown and can generate more connectar to do it#cant say if its my favorite yet bc recency bias is still too fresh but its absolutely my second favorite m&l game at least!!#i havent played paper jam yet i wanted to play the original paper mario and spm first. but i always hear its bad so??#brothership is at least on par with dream team for me rn. absolutely stellar game#i hope this means we'll get more m&l someday! i've already left a very positive response on the survey they put out#anyway. now to decide what to play next because i have a MASSIVE backlog of games and i didnt think this would take this long BJDHJFHF#10/10!!!! please play brothership immediately
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unnormal vivilly dweller thoughts in my head
#“I'm right next to you” are we about to kiss. are you trying to kiss me right neow#i hate the chase sequence part (corny and unoriginal) but everything else is so perfect#hEeEeLP MEeEeEE#i fuckign love vivilly anyway but i think the vivilly dweller is what Really did it fr me#SERIOUSLY THOUGJ WHAT THE FUCK#i would make a palpers dweller but i dont think my computer can with how shit it is rn#like i definitely will at some point (unless someone beats me to it) but i just can't rn 😭#i csnt wait for august viv face reveal guys!!!! YAY!!!! idc what he looks like he will always be so splinkoid#plus whatever characteristics he has i can kinda just add on to my design to him behind his mask#i color his skin as dark grey just for his mc skin but seeing his snapchat n stuff makes me wanna show him off as rhe eyeblinding man he is#or not! who knows . i have a tendency to do whatever#okay speakijg of his face reveal#i have something i want to explain to the wall#a part of me is hoping he isnt generic conventionally attractive guy 38495839488#the rest of me is neutral because idrc#the reason why is most likely because i would feel a deeper connection to him if we shared similar facial features#it's a good reason i think? but still weird to have because i shouldnt really care what he looks like at all#idk what to expect really but i guess i should be open minded abt it#I JUST. a lot of how i perceive him is through his mc character#that played a big part in how i grew to like him so much#but he ISN'T emo hoodie minecraft shyguy!!!#however i can still enjoy the 'persona' he has online. chill sarcastic insane funny blocky shyguy who does a little (A LOT OF) trolling#anyway back to what i was saying#hope bro isn't majestic as fuck irl#IF IT'S ANYTHING LIKE DREAM I'M GOING TO CRY#DREAM IS MAJESTIC AS FUCK I CANT EVEN WITH THAT MAN#i will be supportive anyway ofc because 1) i dont care even though i just proved that i do 2) i can separate persona from irl person 3)...U#IM SO NORMAL#also we're not goijg toctalkcabou t the dream thing. if youre my irl yoy didnt aee this (PLEASE DONT UNFRIEND ME OELASE#DONT LEAVE JUST FORGER Iなはoops didnt mean to type thatSAID THAT OKAY
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Next Generation Sequencing (NGS) Data Analysis Online Training
🚀 Unlock the power of Next Generation Sequencing (NGS) and elevate your bioinformatics skills with our upcoming training course! ⭐ Why join us? In today’s rapidly evolving world of life sciences, mastering NGS data analysis is essential for cutting-edge research. Our comprehensive training programs are designed to equip you with the skills needed to excel in bioinformatics, whether you’re a beginner or looking to advance your expertise. Registrations Open: ✅ Next-Generation Sequencing Data Analysis ✅ Python & Biopython for Bioinformatics 🗓 Dates NGS Data Analysis: September 17 - October 17, 2024 Python & Biopython: September 17 - October 03, 2024 ⏰ Time: 7:00 PM - 8:00 PM IST 🗓 Registration Closes: September 15, 2024 💻 Mode: Online 🎯 Ready to make a difference in your research? Don't miss out on this opportunity to enhance your bioinformatics skills and open new doors in your career. 👉 𝐒𝐞𝐜𝐮𝐫𝐞 𝐘𝐨𝐮𝐫 𝐒𝐩𝐨𝐭 𝐓𝐨𝐝𝐚𝐲: https://lnkd.in/grUEakiP For more details/queries, contact: [email protected] Feel free to reach out with any questions! #Bioinformatics#NGSDataAnalysis#Python hashtag#Biopython #TrainingCourses#CareerGrowth#BioinformaticsEducation#Students #OnlineCourses #BioinformaticsTools #ComputationalBiology #ScienceInnovation
#bioinformatics#next generation sequencing#ngs#genomics!#transcriptomics#omics#online courses#handsontraining#python#data analysis
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If you see me on Spotify listening to rush limelight 45 times in a row don’t worry about it
#my former managerbestie (SAD!*) is really into prog rock and I’m a casual enjoyer so usually when he puts on his prog rock playlist#I know like. the popular stuff kinda well and I recognize a song here and there but whenever this one comes on I suddenly know every word#and he just looks at me slightly confused#Brother 18% of my Spotify top100 was all songs off a playlist I made of songs that remind me of a comic book character#I like to listen to songs and rotate him in my mind. You wouldn’t get it. Well you might#this man is like the first person I’ve met who’s got more ‘was raised on another planet’ vibes#than I have#He will do something insane like have all the clocks in his house set 24 minutes fast#or pour a bowl of cereal and wait 10 minutes so it gets maximum soggy#and be like umm it’s just because I wasn’t raised here (USA) and I have to be like. Dude I know other immigrants you are just weird as hell#in general#(*Well there’s other nucleic acids biotech R&D departments that will hire us for our joint next generation sequencing and omics slay)
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The Dawn of Next Generation Sequencing Technologies: A Revolution in Genomic Science
In genomic science, the advent of Next-Generation Sequencing (NGS) technologies has marked a transformative era, radically changing our approach to understanding the complexities of life at a molecular level. NGS, also known as high-throughput sequencing, encompasses several advanced methodologies that enable rapid sequencing of DNA and RNA much more swiftly and cost-effectively than…
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Next-Generation Sequencing | Explore the Technology - Tekmatic
The term "next-generation sequencing" (NGS) refers to high-throughput technologies that can quickly ascertain the sequence of a particular nucleic acid strand, such as DNA or RNA. These tools have changed how we conduct genomics research. "Next-generation sequencing" refers to various technologies that operate according to various operating principles.
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