Scientific development manager/Bioinformatician - Limagrain Vegetable Seeds Genomics Team chez LIMAGRAIN
extensive evaluation of genome annotation tools. leveraging rna-seq data is a key step towards high structural genome annotation
Skip to main content
Scientific development manager/Bioinformatician - Limagrain Vegetable Seeds Genomics Team chez LIMAGRAIN
extensive evaluation of genome annotation tools. leveraging rna-seq data is a key step towards high structural genome annotation
To view or add a comment, sign in
The era of the $100 genome and beyond is here! Learn more about the the UG 100™ platform and how our early access customers have harnessed the power of genomics at scale.
Ultima Genomics launching high-end DNA sequencers that can read genome for $100 Excited to be working with Ultima Genomics on the commercial roll-out of the UG100 later this year! "The sequencer, dubbed the UG 100, is a $1.5 million machine that can read up to 20,000 human genomes a year. The reagents required to operate the instrument cost as little as $1 per billion sequenced DNA bases; that translates to $100 per genome" https://lnkd.in/eGfMKff6 #FOGBoston2024 #humangenome #nextgenerationsequencing
To view or add a comment, sign in
Faster and Cheaper Genome Sequencing will lead to genomic data tsunami, how can we surf on it instead of being crushed? Embracing artificial intelligence is key to navigating the influx of genomic data.
To view or add a comment, sign in
Ultima Genomics launching high-end DNA sequencers that can read genome for $100 Excited to be working with Ultima Genomics on the commercial roll-out of the UG100 later this year! "The sequencer, dubbed the UG 100, is a $1.5 million machine that can read up to 20,000 human genomes a year. The reagents required to operate the instrument cost as little as $1 per billion sequenced DNA bases; that translates to $100 per genome" https://lnkd.in/eGfMKff6 #FOGBoston2024 #humangenome #nextgenerationsequencing
To view or add a comment, sign in
Director-level executive with experience in Product Strategy / Business Development / Project Management | Passionate about innovation in Biotech / Techbio / Immuno-Oncology / Cell & Gene Therapy
Here comes the $100 genome!
Ultima Genomics launching high-end DNA sequencers that can read genome for $100 Excited to be working with Ultima Genomics on the commercial roll-out of the UG100 later this year! "The sequencer, dubbed the UG 100, is a $1.5 million machine that can read up to 20,000 human genomes a year. The reagents required to operate the instrument cost as little as $1 per billion sequenced DNA bases; that translates to $100 per genome" https://lnkd.in/eGfMKff6 #FOGBoston2024 #humangenome #nextgenerationsequencing
To view or add a comment, sign in
Graphic Designer || Teaching Assistant (University of Cape Coast) || Medical Laboratory Scientist || Academic Data Analyst
As a Medical Laboratory Scientist, I delight in learning modern diagnostic skills. I completed this short course on Genomics and Bioinformatics and it has been an eye opener. I now know how to use the Geneious software to analyze DNA and RNA sequences , identifying patterns and mutation and also developing primers. #genomacinstitute #bioinformatics
To view or add a comment, sign in
🟣 What is a genome code? That's only one of languages - the language which nature uses. All know that AI helps in everyday life to get the crucial message out of the text - and that's perfectly done by AI also for genomic. Check Katerina' s post on AI tools helping professionals to get the essence from genome data 👇👇👇
🟣 3 + 1 𝐀𝐈 𝐭𝐨𝐨𝐥𝐬 for human 𝐠𝐞𝐧𝐨𝐦𝐞 𝐚𝐧𝐚𝐥𝐲𝐬𝐢𝐬. The high-quality products are not for free, but there are some exceptions. 𝐃𝐞𝐞𝐩𝐕𝐚𝐫𝐢𝐚𝐧𝐭 - AI for germline variant-calling in diploid organisms 👉 https://lnkd.in/e2vSHS-A 𝐏𝐚𝐫𝐚𝐛𝐫𝐢𝐜𝐤𝐬 - AI to perform secondary analysis of next-generation sequencing DNA and RNA data 👉 https://lnkd.in/eeP3VtQd 𝐕𝐚𝐫𝐂𝐡𝐚𝐭 - AI assistant for the interpretation of human genomic variations 👉 https://lnkd.in/erWf_d8z Users of 𝐍𝐨𝐯𝐚𝐒𝐞𝐪 and 𝐍𝐞𝐱𝐭𝐒𝐞𝐪 platforms have free access to the newest 𝐃𝐑𝐀𝐆𝐄𝐍 𝐯𝟒.𝟑 - tool for germline and somatic variant calling powered by AI. 👉 https://lnkd.in/e-TbMZVu #illumina #NGS #DRAGEN #GetToKnow
To view or add a comment, sign in
This post might be interesting to Bioinformaticians. Here’s a concise list of tools (updated on January 24, 2024) for the conversion of genomic coordinates between different genome assemblies (like hg19⇄hg38): https://lnkd.in/gskyTRZU #bioinformatics
To view or add a comment, sign in
Genome annotation, neighborhood analysis, and comparative genomics just got a whole lot easier: https://lnkd.in/emFsHV2H https://lnkd.in/eG4XY4-n
To view or add a comment, sign in
🟣 3 + 1 𝐀𝐈 𝐭𝐨𝐨𝐥𝐬 for human 𝐠𝐞𝐧𝐨𝐦𝐞 𝐚𝐧𝐚𝐥𝐲𝐬𝐢𝐬. The high-quality products are not for free, but there are some exceptions. 𝐃𝐞𝐞𝐩𝐕𝐚𝐫𝐢𝐚𝐧𝐭 - AI for germline variant-calling in diploid organisms 👉 https://lnkd.in/e2vSHS-A 𝐏𝐚𝐫𝐚𝐛𝐫𝐢𝐜𝐤𝐬 - AI to perform secondary analysis of next-generation sequencing DNA and RNA data 👉 https://lnkd.in/eeP3VtQd 𝐕𝐚𝐫𝐂𝐡𝐚𝐭 - AI assistant for the interpretation of human genomic variations 👉 https://lnkd.in/erWf_d8z Users of 𝐍𝐨𝐯𝐚𝐒𝐞𝐪 and 𝐍𝐞𝐱𝐭𝐒𝐞𝐪 platforms have free access to the newest 𝐃𝐑𝐀𝐆𝐄𝐍 𝐯𝟒.𝟑 - tool for germline and somatic variant calling powered by AI. 👉 https://lnkd.in/e-TbMZVu #illumina #NGS #DRAGEN #GetToKnow
To view or add a comment, sign in
Create your free account or sign in to continue your search
By clicking Continue to join or sign in, you agree to LinkedIn’s User Agreement, Privacy Policy, and Cookie Policy.
New to LinkedIn? Join now
or
New to LinkedIn? Join now
By clicking Continue to join or sign in, you agree to LinkedIn’s User Agreement, Privacy Policy, and Cookie Policy.