BreakSeek: a breakpoint-based algorithm for full spectral range INDEL detection (Q42552455)

2 November 2017

BreakSeek: a breakpoint-based algorithm for full spectral range INDEL detection (English)

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2 November 2017

Hui Zhao

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2 November 2017

Fangqing Zhao

series ordinal

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2 November 2017

language of work or name

English

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publication date

27 June 2015

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2 November 2017

Nucleic Acids Research

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2 November 2017

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2 November 2017

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2 November 2017

6701-6713

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Creative Commons Attribution-NonCommercial 4.0 International

2 November 2017

start time

8 May 2017

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April 2022 Public Data File from Crossref

copyrighted

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cites work

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28 May 2018

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28 May 2018

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The emerging era of genomic data integration for analyzing splice isoform function

28 May 2018

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28 May 2018

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Systematically differentiating functions for alternatively spliced isoforms through integrating RNA-seq data

28 May 2018

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28 May 2018

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Cancer heterogeneity: implications for targeted therapeutics

28 May 2018

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An integrated map of genetic variation from 1,092 human genomes

28 May 2018

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28 May 2018

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DELLY: structural variant discovery by integrated paired-end and split-read analysis

28 May 2018

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28 May 2018

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Polar and brown bear genomes reveal ancient admixture and demographic footprints of past climate change

28 May 2018

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28 May 2018

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CREST maps somatic structural variation in cancer genomes with base-pair resolution.

28 May 2018

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Natural genetic variation caused by small insertions and deletions in the human genome

28 May 2018

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28 May 2018

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Small insertions and deletions (INDELs) in human genomes

28 May 2018

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

28 May 2018

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Structural variation in the human genome and its role in disease

28 May 2018

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inGAP: an integrated next-generation genome analysis pipeline

28 May 2018

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Computational methods for discovering structural variation with next-generation sequencing

28 May 2018

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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

28 May 2018

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Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

28 May 2018

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Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

28 May 2018

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The Sequence Alignment/Map format and SAMtools

28 May 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

28 May 2018

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Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes

28 May 2018

1 reference

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The diploid genome sequence of an individual human

28 May 2018

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An initial map of insertion and deletion (INDEL) variation in the human genome.

28 May 2018

1 reference

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Structural variation in the human genome

28 May 2018

1 reference

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RSVSim: an R/Bioconductor package for the simulation of structural variations

28 May 2018

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PRISM: pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants

16 August 2018

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Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly

16 August 2018

1 reference

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MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions

16 August 2018

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16 August 2018

Identifiers

DOI

10.1093/NAR/GKV605

1 reference

2 November 2017

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2 November 2017

PubMed publication ID

26117537

1 reference