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Whole-exome sequencing of 17 Brazilian Hereditary Breast Cancer Patients
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创建时间：
2018-11-05
相关数据集
MOESM1 of Mutations in BRCA1, BRCA2 and other breast and ovarian cancer susceptibility genes in Central and South American populations
Additional file 1: Table S1. Cohort characteristics and pathogenic BRCA1 and BRCA2 mutations in hereditary breast cancer in Central and South American populations.
NIAID Data Ecosystem80
Rare exonic mutations identified during the resequencing stage.
Notes: a: Based on NCBI build 37.1. b: Based on NCBI Reference Sequence NC_000020.10. c: Based on NCBI Reference Sequence NP_001099043. AA: amino acid. All mutations are heterozygous. Rare exonic muta
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Homo sapiens Exome. Homo sapiens
Exome sequencing for a Chinese girl with KBG syndrome
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Additional file 9: of Systematic drug screening reveals specific vulnerabilities and co-resistance patterns in endocrine-resistant breast cancer
Point mutations from exome-sequencing. Point mutations, sequencing reads and mutation frequency in tamoxifen-resistant cells (Resistant Reference Reads, Resistant Variant Reads, Resistant Variant Freq
NIAID Data Ecosystem70
Egyptian familial germline mutations
Few relevant studies have been done to address the frequency of germline mutations in Familial Egyptian BC patients and it was only to investigate BRCA1/2 germline profiling. Thus, it was important to
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