A fast and accurate SNP detection algorithm for next-generation sequencing data
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A fast and accurate SNP detection algorithm for next-generation sequencing data
Authors
Keywords
-
Journal
Nature Communications
Volume 3, Issue 1, Pages -
Publisher
Springer Nature
Online
2012-12-04
DOI
10.1038/ncomms2256
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- Genotype and SNP calling from next-generation sequencing data
- (2011) Rasmus Nielsen et al. NATURE REVIEWS GENETICS
- High quality SNP calling using Illumina data at shallow coverage
- (2010) N. Malhis et al. BIOINFORMATICS
- SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
- (2010) Rodrigo Goya et al. BIOINFORMATICS
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- The 1000 Genomes Project: new opportunities for research and social challenges
- (2010) Marc Via et al. Genome Medicine
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- dbSMR: a novel resource of genome-wide SNPs affecting microRNA mediated regulation
- (2009) Manoj Hariharan et al. BMC BIOINFORMATICS
- SNP detection for massively parallel whole-genome resequencing
- (2009) R. Li et al. GENOME RESEARCH
- ssSNPTarget: genome-wide splice-site single nucleotide polymorphism database
- (2009) Jin Ok Yang et al. HUMAN MUTATION
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
- (2009) Ben Langmead et al. GENOME BIOLOGY
- SOAP: short oligonucleotide alignment program
- (2008) R. Li et al. BIOINFORMATICS
- Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing
- (2008) Ryan D. Morin et al. BIOTECHNIQUES
- SNP@Promoter: a database of human SNPs (Single Nucleotide Polymorphisms) within the putative promoter regions
- (2008) Byoung-Chul Kim et al. BMC BIOINFORMATICS
- Mapping short DNA sequencing reads and calling variants using mapping quality scores
- (2008) H. Li et al. GENOME RESEARCH
- Comprehensive genomic characterization defines human glioblastoma genes and core pathways
- (2008) Roger McLendon et al. NATURE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started