- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2105
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Discovering motifs that induce sequencing errors ; volume:14 ; number:5 ; day:10 ; month:4 ; year:2013 ; pages:1-10 ; date:4.2013
BMC bioinformatics ; 14, Heft 5 (10.4.2013), 1-10, 4.2013
- Urheber
-
Allhoff, Manuel
- Beteiligte Personen und Organisationen
-
Schönhuth, Alexander
Martin, Marcel
Costa, Ivan G.
Rahmann, Sven
Marschall, Tobias
SpringerLink (Online service)
- DOI
-
10.1186/1471-2105-14-S5-S1
- URN
-
urn:nbn:de:1111-2016021743900
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:25 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Allhoff, Manuel
- Schönhuth, Alexander
- Martin, Marcel
- Costa, Ivan G.
- Rahmann, Sven
- Marschall, Tobias
- SpringerLink (Online service)
Ähnliche Objekte (12)
Discovering chromatin motifs using FAIRE sequencing and the human diploid genome
Discovering immunoreceptor coupling and organization motifs
Motif-All: discovering all phosphorylation motifs
Discovering multiple realistic TFBS motifs based on a generalized model
The theory of discovering rare variants via DNA sequencing
Sequencing accuracy and systematic errors of nanopore direct RNA sequencing
EMD: an ensemble algorithm for discovering regulatory motifs in DNA sequences
Discovering microRNAs from deep sequencing data using miRDeep
Sequence Bundles: a novel method for visualising, discovering and exploring sequence motifs
Discovering structural motifs using a structural alphabet: Application to magnesium-binding sites
Phenotypic screening of signaling motifs that efficiently induce cell proliferation
Quake: quality-aware detection and correction of sequencing errors
Discovering chromatin motifs using FAIRE sequencing and the human diploid genome
Discovering immunoreceptor coupling and organization motifs
Motif-All: discovering all phosphorylation motifs
Discovering multiple realistic TFBS motifs based on a generalized model
The theory of discovering rare variants via DNA sequencing
Sequencing accuracy and systematic errors of nanopore direct RNA sequencing
EMD: an ensemble algorithm for discovering regulatory motifs in DNA sequences
Discovering microRNAs from deep sequencing data using miRDeep
Sequence Bundles: a novel method for visualising, discovering and exploring sequence motifs
Discovering structural motifs using a structural alphabet: Application to magnesium-binding sites
Phenotypic screening of signaling motifs that efficiently induce cell proliferation
Quake: quality-aware detection and correction of sequencing errors
Discovering chromatin motifs using FAIRE sequencing and the human diploid genome
Discovering immunoreceptor coupling and organization motifs
Motif-All: discovering all phosphorylation motifs
Discovering multiple realistic TFBS motifs based on a generalized model
The theory of discovering rare variants via DNA sequencing
Sequencing accuracy and systematic errors of nanopore direct RNA sequencing
EMD: an ensemble algorithm for discovering regulatory motifs in DNA sequences
Discovering microRNAs from deep sequencing data using miRDeep
Sequence Bundles: a novel method for visualising, discovering and exploring sequence motifs
Discovering structural motifs using a structural alphabet: Application to magnesium-binding sites
Phenotypic screening of signaling motifs that efficiently induce cell proliferation