Detecting large deletions at base pair level by combining split read and paired read data
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2105
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Detecting large deletions at base pair level by combining split read and paired read data ; volume:18 ; number:12 ; day:16 ; month:10 ; year:2017 ; pages:107-113 ; date:10.2017
BMC bioinformatics ; 18, Heft 12 (16.10.2017), 107-113, 10.2017
- Classification
-
Biowissenschaften, Biologie
- Creator
-
Hayes, Matthew
- Contributor
-
Pearson, Jeremy S.
SpringerLink (Online service)
- DOI
-
10.1186/s12859-017-1829-z
- URN
-
urn:nbn:de:1111-2017121121434
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:32 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hayes, Matthew
- Pearson, Jeremy S.
- SpringerLink (Online service)
Other Objects (12)
BreakNet: detecting deletions using long reads and a deep learning approach
Short paired-end reads trump long single-end reads for expression analysis
A sensitive short read homology search tool for paired-end read sequencing data
Accurate indel prediction using paired-end short reads
SOPRA: Scaffolding algorithm for paired reads via statistical optimization
CAREx: context-aware read extension of paired-end sequencing data
Paired-end read length lower bounds for genome re-sequencing
Joining Illumina paired-end reads for classifying phylogenetic marker sequences
READ
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
JAFFAL: detecting fusion genes with long-read transcriptome sequencing
Linked-read sequencing for detecting short tandem repeat expansions
BreakNet: detecting deletions using long reads and a deep learning approach
Short paired-end reads trump long single-end reads for expression analysis
A sensitive short read homology search tool for paired-end read sequencing data
Accurate indel prediction using paired-end short reads
SOPRA: Scaffolding algorithm for paired reads via statistical optimization
CAREx: context-aware read extension of paired-end sequencing data
Paired-end read length lower bounds for genome re-sequencing
Joining Illumina paired-end reads for classifying phylogenetic marker sequences
READ
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
JAFFAL: detecting fusion genes with long-read transcriptome sequencing
Linked-read sequencing for detecting short tandem repeat expansions
BreakNet: detecting deletions using long reads and a deep learning approach
Short paired-end reads trump long single-end reads for expression analysis
A sensitive short read homology search tool for paired-end read sequencing data
Accurate indel prediction using paired-end short reads
SOPRA: Scaffolding algorithm for paired reads via statistical optimization
CAREx: context-aware read extension of paired-end sequencing data
Paired-end read length lower bounds for genome re-sequencing
Joining Illumina paired-end reads for classifying phylogenetic marker sequences
READ
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
JAFFAL: detecting fusion genes with long-read transcriptome sequencing