(Q44245649)

1 December 2017

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

1 reference

1 December 2017

4

Michael Brudno

1 reference

PubMed ID

19483690

1 December 2017

Fereydoun Hormozdiari

series ordinal

2

object named as

Fereydoun Hormozdiari

1 reference

1 December 2017

Seunghak Lee

1

1 reference

PubMed ID

19483690

1 December 2017

Can Alkan

series ordinal

3

1 reference

1 December 2017

31 May 2009

1 reference

1 December 2017

1 reference

1 December 2017

6

1 reference

1 December 2017

473-474

1 reference

1 December 2017

7

1 reference

https://scigraph.springernature.com/pub.10.1038/nmeth.f.256

1 December 2017

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.F.256

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/10.1038%2FNMETH.F.256

A robust framework for detecting structural variations in a genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.F.256

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.F.256

Accurate whole human genome sequencing using reversible terminator chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.F.256

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNMETH.F.256

21 January 2018

Identifiers

DOI

10.1038/NMETH.F.256

1 reference

1 December 2017

1 reference

PubMed ID

19483690