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The human genome has been sequenced in a record time using ultra-rapid nanopore sequencing technology developed by Euan Ashley's team at Stanford Medicine. PacBio has announced the availability of Kinnex kits for full-length RNA sequencing, which enable cutting-edge genomics research. The kits provide scalable and cost-effective sequencing, resolving complex isoforms with high accuracy. NVIDIAHealth has introduced Parabricks 4.2, which offers accelerated workflows for nanopore sequencing and deep learning variant calling. RazorAlign has developed a high-fidelity consensus sequencing method for short reads, as well as a secure data access and de novo transcript assembly protocol. The Quartet Data Portal has been launched, integrating community-wide resources for multiomics quality control. RazorAlign has also introduced a linked-pair long-read sequencing strategy for targeted resequencing and enrichment, and a secure data access and de novo transcript assembly protocol adopting a blockchain-based strategy.
SecDATA, an optimized pipeline for de novo transcript assembly that adopts a Blockchain-based strategy. The major focus here lies towards implementing (a) a pipeline that accesses secured data with the help of DLT and (b) performs de novo transcript sequence reconstruction.
SecDATA: Secure Data Access and de novo Transcript Assembly protocol - To meet the challenge of reliable NGS data analysis https://t.co/KpCXm76vDB https://t.co/dfyLSaDJaq
Linked-Pair Long-Read Sequencing Strategy for Targeted Resequencing and Enrichment https://t.co/FgqV0CthOe https://t.co/Tjs7ADSBY3
High-fidelity (repeat) consensus sequences from short reads using combined read clustering and assembly https://t.co/y3LTkQzOoQ https://t.co/Pc05DPK3HY
The Quartet Data Portal: integration of community-wide resources for multiomics quality control https://t.co/ddJ1CPdO9U https://t.co/muHBKVJozS
SecDATA: Secure Data Access and de novo TranscriptAssembly protocol - To meet the challenge of reliableNGS data analysis https://t.co/QYaEdg49QJ #biorxiv_bioinfo
Genomic Sequencing Advancements with #Parabricks 4.2 introduces accelerated workflows for Oxford Nanopore, NVIDIA GPU compatibility, and deep learning variant calling, empowering diverse sequencer data analysis. #genomics #ai https://t.co/M8VWhWjbxR
The future of RNA sequencing is with long reads! Check out these helpful resources on the new Kinnex RNA kits: https://t.co/HhGlAVlhmM #PacBio #ASHG23 #ASHG2023
Kinnex single-cell RNA kits provide full-length isoform information and single-cell tag formation with high accuracy. Learn more with our new app note: https://t.co/BV4urLZFaf #PacBio #ASHG23 #ASHG2023 https://t.co/CZiTnkpGL0
Kinnex full-length RNA kits provide scalable, cost-effective full-length RNA sequencing. The key difference between short reads? Short reads cannot resolve complex isoforms; HiFi long reads can with extraordinary accuracy. https://t.co/ZSoOvre9wd #PacBio #ASHG23 #ASHG2023 https://t.co/XgcnvA0F2O
Say goodbye to yesterday’s RNA-Seq — say hello to Kinnex. Explore the cost-effective, scalable RNA solutions provided by the new Kinnex kits. https://t.co/xnDfn0KBej #PacBio #ASHG23 #ASHG2023 https://t.co/3sTWz8LIi0
High-fidelity (repeat) consensus sequences from short reads using combined read clustering and assembly https://t.co/y3LTkQzOoQ https://t.co/sWbvWUg2oD
Our new Kinnex kits for full-length #RNA, single-cell RNA, and 16S rRNA sequencing are now available for pre-order, for the Sequel II/ IIe and #Revio systems. Learn how these groundbreaking kits will enable cutting edge #genomics research: https://t.co/RYXEw70H0V #PacBio #ASHG23… https://t.co/g2OBAqwjVD https://t.co/iwRhmM0RzS
From weeks to a matter of hours... The human genome has been sequenced in a new record time, thanks to an ultra-rapid technique developed by @euanashley's team at @StanfordMed, using #nanopore sequencing technology. Learn more: https://t.co/m1AOuy6Wp2 #ASHG23 #wymm