(Q33704815)

28 July 2017

SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data (English)

1 reference

28 July 2017

Nils Becker

3

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author name string

Haley J Abel

1

1 reference

28 July 2017

Eric J Duncavage

2

1 reference

28 July 2017

Jon R Armstrong

4

1 reference

28 July 2017

Vincent J Magrini

5

1 reference

28 July 2017

John D Pfeifer

6

1 reference

28 July 2017

language of work or name

English

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publication date

27 September 2010

1 reference

28 July 2017

1 reference

28 July 2017

26

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28 July 2017

2684-2688

1 reference

28 July 2017

21

1 reference

Basic local alignment search tool

28 July 2017

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Prevalence of Merkel cell polyomavirus in Merkel cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Bootstrap Methods: Another Look at the Jackknife

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Mapping short DNA sequencing reads and calling variants using mapping quality scores

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Target-enrichment strategies for next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Next-generation DNA sequencing methods

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Recurring mutations found by sequencing an acute myeloid leukemia genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

The impact of translocations and gene fusions on cancer causation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Identification of common molecular subsequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

Complex landscapes of somatic rearrangement in human breast cancer genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ528

10.1093/BIOINFORMATICS/BTQ528

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/AbelDBAMP10

28 July 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference