- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1474-760X
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Hidden biases in germline structural variant detection ; volume:22 ; number:1 ; day:20 ; month:12 ; year:2021 ; pages:1-15 ; date:12.2021
Genome biology ; 22, Heft 1 (20.12.2021), 1-15, 12.2021
- Urheber
-
Khayat, Michael M.
Sahraeian, Sayed Mohammad Ebrahim
Zarate, Samantha
Carroll, Andrew
Hong, Huixiao
Pan, Bohu
Shi, Leming
Gibbs, Richard A.
Mohiyuddin, Marghoob
Zheng, Yuanting
Sedlazeck, Fritz
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13059-021-02558-x
- URN
-
urn:nbn:de:101:1-2022041419270658738059
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 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
- Khayat, Michael M.
- Sahraeian, Sayed Mohammad Ebrahim
- Zarate, Samantha
- Carroll, Andrew
- Hong, Huixiao
- Pan, Bohu
- Shi, Leming
- Gibbs, Richard A.
- Mohiyuddin, Marghoob
- Zheng, Yuanting
- Sedlazeck, Fritz
- SpringerLink (Online service)
Ähnliche Objekte (12)
Germline variant affecting p53β isoforms predisposes to familial cancer
Common germline-somatic variant interactions in advanced urothelial cancer
Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
Phenotypic evaluation of deep learning models for classifying germline variant pathogenicity
Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls
Familial acute aortic dissection associated with a novel ACTA2 germline variant
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
Variant detection sensitivity and biases in whole genome and exome sequencing
Germline contamination and leakage in whole genome somatic single nucleotide variant detection
Accuracy and efficiency of germline variant calling pipelines for human genome data
Inferring structural variant cancer cell fraction
Germline variant affecting p53β isoforms predisposes to familial cancer
Common germline-somatic variant interactions in advanced urothelial cancer
Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
Phenotypic evaluation of deep learning models for classifying germline variant pathogenicity
Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls
Familial acute aortic dissection associated with a novel ACTA2 germline variant
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
Variant detection sensitivity and biases in whole genome and exome sequencing
Germline contamination and leakage in whole genome somatic single nucleotide variant detection
Accuracy and efficiency of germline variant calling pipelines for human genome data
Inferring structural variant cancer cell fraction
Germline variant affecting p53β isoforms predisposes to familial cancer
Common germline-somatic variant interactions in advanced urothelial cancer
Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
Phenotypic evaluation of deep learning models for classifying germline variant pathogenicity
Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls
Familial acute aortic dissection associated with a novel ACTA2 germline variant
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
Variant detection sensitivity and biases in whole genome and exome sequencing
Germline contamination and leakage in whole genome somatic single nucleotide variant detection
Accuracy and efficiency of germline variant calling pipelines for human genome data