(Q48552967)

12 February 2018

title

RSVSim: an R/Bioconductor package for the simulation of structural variations. (English)

1 reference

12 February 2018

inferred from name or label

main subject

R package

1 reference

based on heuristic

7 September 2021

author name string

Christoph Bartenhagen

series ordinal

1

1 reference

12 February 2018

Martin Dugas

series ordinal

2

1 reference

12 February 2018

language of work or name

English

0 references

publication date

25 April 2013

1 reference

12 February 2018

published in

Bioinformatics

1 reference

12 February 2018

volume

29

1 reference

12 February 2018

issue

13

1 reference

12 February 2018

page(s)

1679-1681

1 reference

12 February 2018

Genome structural variation discovery and genotyping

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

FUSIM: a software tool for simulating fusion transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Mapping translocation breakpoints by next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

pIRS: Profile-based Illumina pair-end reads simulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

CLEVER: clique-enumerating variant finder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Mechanisms of formation of structural variation in a fully sequenced human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

Detecting structural variations in the human genome using next generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT198

10.1093/BIOINFORMATICS/BTT198

21 January 2018

Identifiers

DOI

1 reference

12 February 2018

journals/bioinformatics/BartenhagenD13

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

12 February 2018