Posts Tagged ‘i01kgsv15’

Characterization of structural variants with single molecule and hybrid sequencing approaches

Saturday, May 16th, 2015

Characterization of #SVs w. single molecule & hybrid sequencing http://bioinformatics.oxfordjournals.org/content/30/24/3458.abstract Probabilistic read mapping, re-evaluating adjacencies

QT:{{"
We present MultiBreak-SV, an algorithm to detect structural variants
(SVs) from single molecule sequencing data, paired read sequencing
data, or a combination of sequencing data from different platforms.
"}}

What is it? · iobio

Monday, May 4th, 2015

http://iobio.io/

remills / SVelter — Bitbucket

Monday, May 4th, 2015

https://bitbucket.org/remills/svelter

Notes from JAX structural variation meeting

Monday, May 4th, 2015

http://linkstream2.gerstein.info/tag/i01kgsv15/

What is it? · iobio

Monday, May 4th, 2015

Viz of datasets

http://iobio.io/

remills / SVelter — Bitbucket

Monday, May 4th, 2015

https://bitbucket.org/remills/svelter

predict bkpts & assess

BMC Genomics | Abstract | Assessing structural variation in a personal genome—towards a human reference d iploid genome

Monday, May 4th, 2015

consensus method

http://www.biomedcentral.com/1471-2164/16/286/abstract

Genome Biology | Full text | An integrative probabilistic model for identification of structural variation in sequencing data

Monday, May 4th, 2015

QT:{{”
We introduce GASVPro, an algorithm combining both paired read and read depth signals into a probabilistic model that can analyze multiple alignments of reads.
“}}

http://genomebiology.com/2012/13/3/R22

Characterization of structural variants with single molecule and hybrid sequencing approaches

Monday, May 4th, 2015

QT:{{”
We present MultiBreak-SV, an algorithm to detect structural variants (SVs) from single molecule sequencing data, paired read sequencing data, or a combination of sequencing data from different platforms. “}}

uses pacbio

http://bioinformatics.oxfordjournals.org/content/30/24/3458.long