"Germline sequencing" trang 1 - tải miễn phí từ tailieuXANH
Germline and somatic mutations in patients with multiple primary melanomas: A next generation sequencing study

Germline and somatic mutations in patients with multiple primary melanomas: A next generation sequencing study
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Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection
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The PiGeOn project: Protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer

The PiGeOn project: Protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer
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A germline mutation in Rab43 gene identified from a cancer family predisposes to a hereditary liver-colon cancer syndrome

A germline mutation in Rab43 gene identified from a cancer family predisposes to a hereditary liver-colon cancer syndrome
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Long-term health and germline transmission in transgenic cattle following transposonmediated gene transfer

Long-term health and germline transmission in transgenic cattle following transposonmediated gene transfer
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Germline whole exome sequencing of a family with appendiceal mucinous tumours presenting with pseudomyxoma peritonei

Germline whole exome sequencing of a family with appendiceal mucinous tumours presenting with pseudomyxoma peritonei
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Substantial batch effects in TCGA exome sequences undermine pan-cancer analysis of germline variants

Substantial batch effects in TCGA exome sequences undermine pan-cancer analysis of germline variants
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Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil

Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil
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The PiGeOn project: protocol for a longitudinal study examining psychosocial, behavioural and ethical issues and outcomes in cancer tumour genomic profiling

The PiGeOn project: protocol for a longitudinal study examining psychosocial, behavioural and ethical issues and outcomes in cancer tumour genomic profiling
10    44    0
Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patients

Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patients
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Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk

Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk
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Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia

Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia
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FAVR (Filtering and Annotation of Variants that are Rare): Methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets

FAVR (Filtering and Annotation of Variants that are Rare): Methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets
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Hidden biases in germline structural variant detection

Hidden biases in germline structural variant detection
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Germline variation networks in the PI3K/ AKT pathway corresponding to familial high-incidence lung cancer pedigrees

Germline variation networks in the PI3K/ AKT pathway corresponding to familial high-incidence lung cancer pedigrees
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Mutation landscape of germline and somatic BRCA1/2 in patients with highgrade serous ovarian cancer

Mutation landscape of germline and somatic BRCA1/2 in patients with highgrade serous ovarian cancer
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Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria
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Genome instability in blood cells of a BRCA1+ breast cancer family

Genome instability in blood cells of a BRCA1+ breast cancer family
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Comprehensive analysis of germline mutations in northern Brazil: A panel of 16 genes for hereditary cancer-predisposing syndrome investigation

Comprehensive analysis of germline mutations in northern Brazil: A panel of 16 genes for hereditary cancer-predisposing syndrome investigation
8    37    1
Spectrum of Germline RET variants identified by targeted sequencing and associated Multiple Endocrine Neoplasia type 2 susceptibility in China

Spectrum of Germline RET variants identified by targeted sequencing and associated Multiple Endocrine Neoplasia type 2 susceptibility in China
17    35    1
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