- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2105
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
WEP: a high-performance analysis pipeline for whole-exome data ; volume:14 ; number:7 ; day:22 ; month:4 ; year:2013 ; pages:1-11 ; date:4.2013
BMC bioinformatics ; 14, Heft 7 (22.4.2013), 1-11, 4.2013
- Creator
-
D'Antonio, Mattia
- Contributor
-
D'Onorio De Meo, Paolo
Paoletti, Daniele
Elmi, Berardino
Pallocca, Matteo
Sanna, Nico
Picardi, Ernesto
Pesole, Graziano
Castrignanò, Tiziana
SpringerLink (Online service)
- DOI
-
10.1186/1471-2105-14-S7-S11
- URN
-
urn:nbn:de:1111-2016021744226
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:35 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
- D'Antonio, Mattia
- D'Onorio De Meo, Paolo
- Paoletti, Daniele
- Elmi, Berardino
- Pallocca, Matteo
- Sanna, Nico
- Picardi, Ernesto
- Pesole, Graziano
- Castrignanò, Tiziana
- SpringerLink (Online service)
Other Objects (12)
Whole-exome sequencing of a pedigree segregating asthma
Readability of informed consent forms for whole-exome and whole-genome sequencing
Comprehensive comparison of three commercial human whole-exome capture platforms
Genomic alterations in gastric cancers discovered via whole-exome sequencing
Human whole-exome genotype data for Alzheimer’s disease
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation
Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration
Whole-exome sequencing reveals the origin and evolution of hepato-cholangiocarcinoma
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Whole-exome sequencing of a pedigree segregating asthma
Readability of informed consent forms for whole-exome and whole-genome sequencing
Comprehensive comparison of three commercial human whole-exome capture platforms
Genomic alterations in gastric cancers discovered via whole-exome sequencing
Human whole-exome genotype data for Alzheimer’s disease
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation
Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration
Whole-exome sequencing reveals the origin and evolution of hepato-cholangiocarcinoma
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Whole-exome sequencing of a pedigree segregating asthma
Readability of informed consent forms for whole-exome and whole-genome sequencing
Comprehensive comparison of three commercial human whole-exome capture platforms
Genomic alterations in gastric cancers discovered via whole-exome sequencing
Human whole-exome genotype data for Alzheimer’s disease
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation
Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration
Whole-exome sequencing reveals the origin and evolution of hepato-cholangiocarcinoma