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[HTML][HTML] CNVkit: genome-wide copy number detection and visualization from targeted DNA sequencing

E Talevich, AH Shain, T Botton… - PLoS computational …, 2016 - journals.plos.org
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …
被引用次数：1553 相关文章

[引用][C] CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton… - PLOS Computational …, 2016 - cir.nii.ac.jp
CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA
Sequencing | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 …

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.

E Talevich, AH Shain, T Botton… - Plos Computational …, 2016 - europepmc.org
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton… - PLOS Computational …, 2016 - escholarship.org
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton… - PLoS Computational …, 2016 - search.proquest.com
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton… - PLoS Computational …, 2016 - go.gale.com
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton… - PLoS computational …, 2016 - pubmed.ncbi.nlm.nih.gov
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …
[PDF] researchgate.net

[PDF][PDF] CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton, BC Bastian - PLoS Comput Biol, 2016 - researchgate.net
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …
[HTML] nih.gov

[HTML][HTML] CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing

E Talevich, AH Shain, T Botton… - PLoS Computational …, 2016 - ncbi.nlm.nih.gov
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …

CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.

E Talevich, AH Shain, T Botton, BC Bastian - 2016 - agris.fao.org
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are
of significant importance in syndromic conditions and cancer. Massively parallel sequencing …