Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. (Q34124844)

31 July 2017

Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. (English)

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31 July 2017

6

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31 July 2017

Stefan A Haas

7

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Martin Vingron

5

object named as

Martin Vingron

1 reference

31 July 2017

4

Ruping Sun

1 reference

31 July 2017

Anne-Katrin Emde

1

1 reference

31 July 2017

Marcel H Schulz

2

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31 July 2017

David Weese

3

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31 July 2017

Knut Reinert

8

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31 July 2017

language of work or name

English

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publication date

11 January 2012

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31 July 2017

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31 July 2017

28

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31 July 2017

5

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31 July 2017

619-627

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Dindel: accurate indel calls from short-read data

31 July 2017

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Genome structural variation discovery and genotyping

21 January 2018

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Global and unbiased detection of splice junctions from RNA-seq data

21 January 2018

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Detection of splice junctions from paired-end RNA-seq data by SpliceMap.

21 January 2018

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High-resolution profiling of histone methylations in the human genome

21 January 2018

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Accurate whole human genome sequencing using reversible terminator chemistry

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Mapping translocation breakpoints by next-generation sequencing

21 January 2018

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

21 January 2018

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SeqAn an efficient, generic C++ library for sequence analysis

21 January 2018

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A map of human genome variation from population-scale sequencing

21 January 2018

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Real-time DNA sequencing from single polymerase molecules

21 January 2018

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A Draft Sequence of the Neandertal Genome

21 January 2018

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Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA.

21 January 2018

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Detection of large-scale variation in the human genome

21 January 2018

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Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate

21 January 2018

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Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

21 January 2018

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PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data

21 January 2018

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Microindel detection in short-read sequence data

21 January 2018

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

21 January 2018

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Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly

21 January 2018

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Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

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

21 January 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

21 January 2018

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Computational methods for discovering structural variation with next-generation sequencing

21 January 2018

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Sequencing technologies - the next generation

21 January 2018

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Mapping copy number variation by population-scale genome sequencing

21 January 2018

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

21 January 2018

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Small insertions and deletions (INDELs) in human genomes

21 January 2018

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A fast bit-vector algorithm for approximate string matching based on dynamic programming

21 January 2018

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Targeted capture and massively parallel sequencing of 12 human exomes

21 January 2018

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Array comparative genomic hybridization and its applications in cancer

21 January 2018

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dbSNP: the NCBI database of genetic variation

21 January 2018

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Structural variation in the human genome and its role in disease

21 January 2018

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The Human Gene Mutation Database: 2008 update

21 January 2018

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Exploring the genomes of cancer cells: progress and promise

21 January 2018

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RNA-Seq: a revolutionary tool for transcriptomics

21 January 2018

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MapSplice: accurate mapping of RNA-seq reads for splice junction discovery.

21 January 2018

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RazerS--fast read mapping with sensitivity control

21 January 2018

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The complete genome of an individual by massively parallel DNA sequencing

21 January 2018

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

21 January 2018

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CNV-seq, a new method to detect copy number variation using high-throughput sequencing

21 January 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

21 January 2018

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Sensitive and accurate detection of copy number variants using read depth of coverage

21 January 2018

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SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data

21 January 2018

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10.1093/BIOINFORMATICS/BTS019

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/EmdeSWSVKHR12

31 July 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference