Pulse Explorar nav.journalClub Debates Tendencias Investigadores Revistas

Join discussions, follow papers, and never miss your next session.

Download on theApp Store

Inicio Explorar nav.journalClub Tendencias

⌘+K

Fast and SNP-tolerant detection of complex variants and splicing in short reads | Synapse

February 10, 2010Open Access

Ver artículo completo

Fast and SNP-tolerant detection of complex variants and splicing in short reads

TWThomas D. WuGuangxi University ŞNŞerban NacuUniversity of California System

Puntos clave

Los puntos clave no están disponibles para este artículo en este momento.

Resumen

Source code in C and utility programs in Perl are freely available for download as part of the GMAP package at http://share.gene.com/gmap.

Preguntar a la IA

Me gusta

Guardar

Compartir

Ver artículo completo

Cite This Study

Wu et al. (Wed,) studied this question.

synapsesocial.com/papers/69a011ada5a27806a00b5f30 https://doi.org/https://doi.org/10.1093/bioinformatics/btq057

Preguntar a la IA

Me gusta

Guardar

Compartir

Ver artículo completo

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Fast and accurate short read alignment with Burrows–Wheeler transform2009 · 63,475 citations
2Locus-specific control of asymmetric and CpNpG methylation by the <i>DRM</i> and <i>CMT3</i> methyltransferase genes2002 · 568 citations
3Evaluation of DNA microarray results with quantitative gene expression platforms2006 · 620 citations
4dbSNP: the NCBI database of genetic variation2001 · 7,908 citations
5Alternative isoform regulation in human tissue transcriptomes2008 · 5,391 citations