Applications and analysis of targeted genomic sequencing in cancer studies.
Comput Struct Biotechnol J
; 17: 1348-1359, 2019.
Article
en En
| MEDLINE
| ID: mdl-31762958
BAM, Binary Alignment Map; BWA, Burrows-Wheeler Aligner; Background error; CLL, Chronic Lymphocytic Leukaemia; COSMIC, Catalogue of Somatic Mutations in Cancer; Cancer genomics; Clinical samples; ESP, Exome Sequencing Project; FF, Fresh Frozen; FFPE, Formalin Fixed Paraffin Embedded; FL, Follicular Lymphoma; GATK, Genome Analysis Toolkit; ICGC, International Cancer Genome Consortium; MBC, Molecular Barcode; NCCN, the National Comprehensive Cancer Network®; NGS, Next Generation Sequencing; NHL, Non-Hodgkin Lymphoma; NSCLC, Non-Small Cell Lung Carcinoma; PCR duplicates; QC, Quality Control; SAM, Sequence Alignment Map; TCGA, The Cancer Genome Atlas; TS, Targeted Sequencing; Targeted sequencing; UMI, Unique Molecular Identifiers; VAF, Variant Allele Frequency; Variant calling; WES, Whole Exome Sequencing; WGS, Whole Genome Sequencing; tFL, Transformed Follicular Lymphoma
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Tipo de estudio:
Guideline
Idioma:
En
Revista:
Comput Struct Biotechnol J
Año:
2019
Tipo del documento:
Article
País de afiliación:
Reino Unido
Pais de publicación:
Países Bajos