STORMSeq: an open-source, user-friendly pipeline for processing personal genomics data in the cloud. - Wikidata - awgldk - TriplyDB

STORMSeq: an open-source, user-friendly pipeline for processing personal genomics data in the cloud.

STORMSeq: an open-source, user-friendly pipeline for processing personal genomics data in the cloud.

http://www.wikidata.org/entity/Q30486640

about

Fastq2vcf: a concise and transparent pipeline for whole-exome sequencing data analyses Clinical Genomics: Challenges and Opportunities PVT: an efficient computational procedure to speed up next-generation sequence analysis.Inexpensive and Highly Reproducible Cloud-Based Variant Calling of 2,535 Human Genomes.Tentacle: distributed quantification of genes in metagenomes.Scalable and cost-effective NGS genotyping in the cloud.MC-GenomeKey: a multicloud system for the detection and annotation of genomic variants.IMPACT: a whole-exome sequencing analysis pipeline for integrating molecular profiles with actionable therapeutics in clinical samples.Interpreting functional effects of coding variants: challenges in proteome-scale prediction, annotation and assessment.Cloud-based Interactive Analytics for Terabytes of Genomic Variants Data.

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P2860

STORMSeq: an open-source, user-friendly pipeline for processing personal genomics data in the cloud.

http://www.wikidata.org/entity/Q30486640

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

@zh-hk

2014年論文

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2014年論文

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2014年论文

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name

STORMSeq: an open-source, user ...... al genomics data in the cloud.

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STORMSeq: an open-source, user ...... al genomics data in the cloud.

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STORMSeq: an open-source, user ...... al genomics data in the cloud.

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Guy Haskin Fernald

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Joel T Dudley

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Michael Snyder

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P2860

Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences

Fast and accurate short read alignment with Burrows-Wheeler transform

The Sequence Alignment/Map format and SAMtools

ggbio: an R package for extending the grammar of graphics for genomic data

A framework for variation discovery and genotyping using next-generation DNA sequencing data

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

D³: Data-Driven Documents.

SIMPLEX: cloud-enabled pipeline for the comprehensive analysis of exome sequencing data.

Searching for SNPs with cloud computing.

Interpretome: a freely available, modular, and secure personal genome interpretation engine

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e84860

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Nicholas P. Tatonetti

Konrad J. Karczewski

Alicia R Martin

Jakub Karczewski

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open-source software

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