MtDNA Position Conversions - SNPedia
The most widely used mtDNA reference sequence in use at this writing is the Revised Cambridge Reference Sequence (rCRS), and is the reference sequence for the human genome build 37 reference. The newer Reconstructed Sapiens Reference Sequence (RSRS) is expected to become the preferred reference sequence, as it is a psuedo-sequence representing what is assumed the earliest human's mtDNA sequence wo
Existing Workflow systems
Permalink: https://s.apache.org/existing-workflow-systems Cite as (update dates): Peter Amstutz, Maxim Mikheev, Michael R. Crusoe, Nebojša Tijanić, Samuel Lampa, et al. (2022): Existing Workflow systems. Common Workflow Language wiki, GitHub. https://s.apache.org/existing-workflow-systems updated 2023-11-23, accessed 2023-11-23. Computational Data Analysis Workflow Systems An incomplete list Pleas
Cloudera、ブロード研究所と次世代ゲノム解析ツールキットを開発
Cloudera、ブロード研究所と次世代ゲノム解析ツールキットを開発Apache Sparkを使用しCloudera Enterprise上でバイオインフォマティクス（生物情報学）の スタンダードとして、ゲノム研究の促進に向けデザインされたGATK4を開発 2016年4月6日 米国カリフォルニア州パロアルト発 － Apache Hadoopと最新のオープンソーステクノロジーをベースに、最も高速で最も使いやすく、セキュアなデータ管理と分析を実現するプラットフォームを提供するClouderaは、本日、生物医学とゲノム研究の世界最先端をいくマサチューセッツ工科大およびハーバード大の研究施設のブロード研究所との協業を発表しました。２つの組織は、次世代のゲノム解析ツールキット“GATK4"の開発を推進するために、今年度共同で作業を行います。 Cloudera Enterpriseは、臨床医や研究者お
Three ways to trim adaptor/primer sequences for paired-end reads
My learning notes for R, Unix, Perl, statistics, tools/resources, biology etc. everything about Bioinformatics 1. Understanding the adaptors (skip this part if you're familiar with the Illumina adaptor) Before trimming anything from the reads, let's get clear what the reads content is. Taking Trufseq reads (from Illumina HiSeq 2000) as example, here is the read file (fastq) looks like: $ cat r1.fq
Secure & powerful custom BLAST analysis servers for your team and data
Empowering biologists with intuitive custom BLAST servers since 2011 Run BLAST on standard or custom data: Join >20,000 users and experience the power of SequenceServer Get Started Today Researchers and staff scientists in hundreds of companies and labs use SequenceServer to BLAST their data, with more than 200 citations. Applications range from vaccine development to cancer research, molecular di
リリース、障害情報などのサービスのお知らせ
最新の人気エントリーの配信
j次のブックマーク
k前のブックマーク
lあとで読む
eコメント一覧を開く
oページを開く
LeafCutter vs. MAJIQ and comparing differential splicing algorithms
GitHub - pbnjay/lollipops: This is the development fork - Stable code has been moved to ==>
Improving genetic diagnosis in Mendelian disease with transcriptome sequencing – a walk through
rCRS vs. RSRS vs. HG19 (Yoruba) | Haplogrep
Automatic IGV snapshot script
How To Create Mutation Diagram In R Or In Any Tools?
(Modern, mid-2016) RNA-seq software pipeline
Guideline to bioinformatics tools
RCSB PDB - Browse Human Genes
Which Bioinformatic Friendly Pipeline Building Framework?
Using Kallisto for expression analysis of published RNAseq data | Bench to Bioinformatics
Home - rawcopy
FermiKit: assembly-based variant calling for Illumina resequencing data
Genome Coordinate Conventions
dustbox-web.com || TOP