Inferring copy number and genotype in tumour exome data

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2164

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Inferring copy number and genotype in tumour exome data ; volume:15 ; number:1 ; day:28 ; month:8 ; year:2014 ; pages:1-12 ; date:12.2014
BMC genomics ; 15, Heft 1 (28.8.2014), 1-12, 12.2014

Creator: Amarasinghe, Kaushalya C.

Contributor: Li, Jason
Hunter, Sally M.
Ryland, Georgina L.
Cowin, Prue A.
Campbell, Ian G.
Halgamuge, Saman K.
SpringerLink (Online service)

DOI: 10.1186/1471-2164-15-732

URN: urn:nbn:de:1111-201607293662

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:48 AM CEST

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Amarasinghe, Kaushalya C.
Li, Jason
Hunter, Sally M.
Ryland, Georgina L.
Cowin, Prue A.
Campbell, Ian G.
Halgamuge, Saman K.
SpringerLink (Online service)

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Sacral agenesis: a pilot whole exome sequencing and copy number study

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Quantitative model for inferring dynamic regulation of the tumour suppressor gene p53

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Sample-Index Misassignment Impacts Tumour Exome Sequencing

Assessing the reproducibility of exome copy number variations predictions

Identification of copy number variants from exome sequence data

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EXCAVATOR: detecting copy number variants from whole-exome sequencing data

A danger of low copy numbers for inferring incorrect cooperativity degree

Inferring Crohn’s disease association from exome sequences by integrating biological knowledge

Sacral agenesis: a pilot whole exome sequencing and copy number study

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Inferring copy number and genotype in tumour exome data

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Other Objects (12)

Sample-Index Misassignment Impacts Tumour Exome Sequencing

Assessing the reproducibility of exome copy number variations predictions

Identification of copy number variants from exome sequence data

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

A danger of low copy numbers for inferring incorrect cooperativity degree

Inferring Crohn’s disease association from exome sequences by integrating biological knowledge

Sacral agenesis: a pilot whole exome sequencing and copy number study

SCONCE2: jointly inferring single cell copy number profiles and tumor evolutionary distances

Quantitative model for inferring dynamic regulation of the tumour suppressor gene p53

Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome

Sample-Index Misassignment Impacts Tumour Exome Sequencing

Assessing the reproducibility of exome copy number variations predictions

Identification of copy number variants from exome sequence data

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

A danger of low copy numbers for inferring incorrect cooperativity degree

Inferring Crohn’s disease association from exome sequences by integrating biological knowledge

Sacral agenesis: a pilot whole exome sequencing and copy number study

SCONCE2: jointly inferring single cell copy number profiles and tumor evolutionary distances

Quantitative model for inferring dynamic regulation of the tumour suppressor gene p53

Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome

Sample-Index Misassignment Impacts Tumour Exome Sequencing

Assessing the reproducibility of exome copy number variations predictions

Identification of copy number variants from exome sequence data

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

A danger of low copy numbers for inferring incorrect cooperativity degree

Inferring Crohn’s disease association from exome sequences by integrating biological knowledge

Sacral agenesis: a pilot whole exome sequencing and copy number study

SCONCE2: jointly inferring single cell copy number profiles and tumor evolutionary distances

Quantitative model for inferring dynamic regulation of the tumour suppressor gene p53

Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome

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