- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2105
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Joint genotype inference with germline and somatic mutations ; volume:14 ; number:5 ; day:10 ; month:4 ; year:2013 ; pages:1-11 ; date:4.2013
BMC bioinformatics ; 14, Heft 5 (10.4.2013), 1-11, 4.2013
- Urheber
-
Bareke, Eric
- Beteiligte Personen und Organisationen
-
Saillour, Virginie
Spinella, Jean-François
Vidal, Ramón
Healy, Jasmine
Sinnett, Daniel
Csűrös, Miklós
SpringerLink (Online service)
- DOI
-
10.1186/1471-2105-14-S5-S3
- URN
-
urn:nbn:de:1111-2016021743821
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:26 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
- Bareke, Eric
- Saillour, Virginie
- Spinella, Jean-François
- Vidal, Ramón
- Healy, Jasmine
- Sinnett, Daniel
- Csűrös, Miklós
- SpringerLink (Online service)
Ähnliche Objekte (12)
Investigations of somatic and germline mutations in primary aldosteronism
Association between germline variants and somatic mutations in colorectal cancer
Virmid: accurate detection of somatic mutations with sample impurity inference
SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations
Comparison of Germline versus Somatic BAP1 Mutations for Risk of Metastasis in Uveal Melanoma
Origins and characterization of variants shared between databases of somatic and germline human mutations
Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study
First-decade patient with colorectal cancer carrying both germline and somatic mutations in APC gene
Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia
Non-canonical FLT3 alterations reveal novel germline FLT3 variants leading to somatic gene rescue mutations
Population-based statistical inference for temporal sequence of somatic mutations in cancer genomes
Low-level brain somatic mutations in exonic regions are collectively implicated in autism with germline mutations in autism risk genes
Investigations of somatic and germline mutations in primary aldosteronism
Association between germline variants and somatic mutations in colorectal cancer
Virmid: accurate detection of somatic mutations with sample impurity inference
SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations
Comparison of Germline versus Somatic BAP1 Mutations for Risk of Metastasis in Uveal Melanoma
Origins and characterization of variants shared between databases of somatic and germline human mutations
Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study
First-decade patient with colorectal cancer carrying both germline and somatic mutations in APC gene
Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia
Non-canonical FLT3 alterations reveal novel germline FLT3 variants leading to somatic gene rescue mutations
Population-based statistical inference for temporal sequence of somatic mutations in cancer genomes
Low-level brain somatic mutations in exonic regions are collectively implicated in autism with germline mutations in autism risk genes
Investigations of somatic and germline mutations in primary aldosteronism
Association between germline variants and somatic mutations in colorectal cancer
Virmid: accurate detection of somatic mutations with sample impurity inference
SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations
Comparison of Germline versus Somatic BAP1 Mutations for Risk of Metastasis in Uveal Melanoma
Origins and characterization of variants shared between databases of somatic and germline human mutations
Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study
First-decade patient with colorectal cancer carrying both germline and somatic mutations in APC gene
Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia
Non-canonical FLT3 alterations reveal novel germline FLT3 variants leading to somatic gene rescue mutations
Population-based statistical inference for temporal sequence of somatic mutations in cancer genomes