damidseq_pipeline: an automated pipeline for processing DamID sequencing datasets.
dc.contributor.author | Marshall, Owen J | |
dc.contributor.author | Brand, Andrea H | |
dc.date.accessioned | 2015-07-01T13:36:10Z | |
dc.date.available | 2015-07-01T13:36:10Z | |
dc.date.issued | 2015-10-15 | |
dc.identifier.citation | Bioinformatics 2015, 31(20):3371-3373. doi:10.1093/bioinformatics/btv386 | |
dc.identifier.issn | 1367-4803 | |
dc.identifier.uri | https://www.repository.cam.ac.uk/handle/1810/248778 | |
dc.description.abstract | UNLABELLED: DamID is a powerful technique for identifying regions of the genome bound by a DNA-binding (or DNA-associated) protein. Currently, no method exists for automatically processing next-generation sequencing DamID (DamID-seq) data, and the use of DamID-seq datasets with normalization based on read-counts alone can lead to high background and the loss of bound signal. DamID-seq thus presents novel challenges in terms of normalization and background minimization. We describe here damidseq_pipeline, a software pipeline that performs automatic normalization and background reduction on multiple DamID-seq FASTQ datasets. AVAILABILITY AND IMPLEMENTATION: Open-source and freely available from http://owenjm.github.io/damidseq_pipeline. The damidseq_pipeline is implemented in Perl and is compatible with any Unix-based operating system (e.g. Linux, Mac OSX). CONTACT: o.marshall@gurdon.cam.ac.uk SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. | |
dc.description.sponsorship | We thank Charles Bradshaw for helpful comments on the software. This work was supported by the BBSRC [BB/L00786X/1] and Wellcome Trust [092545]. The Gurdon Institute is supported by core funding from the Wellcome Trust [092096] and CRUK [C6946/A14492]. | |
dc.language | English | |
dc.language.iso | en | |
dc.publisher | Oxford University Press (OUP) | |
dc.rights | Attribution 2.0 UK: England & Wales | |
dc.rights.uri | http://creativecommons.org/licenses/by/2.0/uk/ | |
dc.subject | Binding Sites | |
dc.subject | DNA-Binding Proteins | |
dc.subject | High-Throughput Nucleotide Sequencing | |
dc.subject | Sequence Analysis, DNA | |
dc.subject | Software | |
dc.title | damidseq_pipeline: an automated pipeline for processing DamID sequencing datasets. | |
dc.type | Article | |
dc.description.version | This is the final published version. It first appeared at http://dx.doi.org/10.1093/bioinformatics/btv386 | |
prism.endingPage | 3373 | |
prism.publicationDate | 2015 | |
prism.publicationName | Bioinformatics | |
prism.startingPage | 3371 | |
prism.volume | 31 | |
dc.rioxxterms.funder | BBSRC | |
dc.rioxxterms.funder | Wellcome Trust | |
dc.rioxxterms.funder | CRUK | |
dc.rioxxterms.projectid | BB/L00786X/1 | |
dc.rioxxterms.projectid | 092545 | |
dc.rioxxterms.projectid | 092096 | |
dc.rioxxterms.projectid | C6946/A14492 | |
dcterms.dateAccepted | 2015-06-20 | |
rioxxterms.versionofrecord | 10.1093/bioinformatics/btv386 | |
rioxxterms.licenseref.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
rioxxterms.licenseref.startdate | 2015-06-25 | |
dc.contributor.orcid | Brand, Andrea [0000-0002-2089-6954] | |
dc.identifier.eissn | 1367-4811 | |
rioxxterms.type | Journal Article/Review | |
pubs.funder-project-id | Biotechnology and Biological Sciences Research Council (BB/L00786X/1) | |
pubs.funder-project-id | Wellcome Trust (092545/Z/10/Z) | |
pubs.funder-project-id | Wellcome Trust (092096/Z/10/Z) | |
pubs.funder-project-id | Wellcome Trust (103792/Z/14/Z) | |
pubs.funder-project-id | Cancer Research Uk (None) | |
cam.issuedOnline | 2015-06-25 |
Files in this item
This item appears in the following Collection(s)
-
Scholarly Works - Wellcome Trust/Cancer Research UK Gurdon Institute
-
Symplectic mapped items for data match
This collection contains all articles, datasets and conference objects to be harvested