Whole exome sequencing analysis trang 1 tải miễn phí từ tailieunhanh

"Whole exome sequencing analysis" trang 1 - tải miễn phí từ tailieunhanh

NAPG mutation in family members with hereditary hemorrhagic telangiectasia in China

NAPG mutation in family members with hereditary hemorrhagic telangiectasia in China

9 36 1

Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis

Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis

13 40 1

A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

10 20 1

MutEnricher: A flexible toolset for somatic mutation enrichment analysis of tumor whole genomes

MutEnricher: A flexible toolset for somatic mutation enrichment analysis of tumor whole genomes

8 87 1

Comparative sequence analysis of patientmatched primary colorectal cancer, metastatic, and recurrent metastatic tumors after adjuvant FOLFOX chemotherapy

Comparative sequence analysis of patientmatched primary colorectal cancer, metastatic, and recurrent metastatic tumors after adjuvant FOLFOX chemotherapy

11 42 1

The mutational burden and oligogenic inheritance in Klippel-Feil syndrome

The mutational burden and oligogenic inheritance in Klippel-Feil syndrome

9 27 1

Mutational concordance analysis provides supportive information for double cancer diagnosis

Mutational concordance analysis provides supportive information for double cancer diagnosis

7 28 1

Lower PRDM2 expression is associated with dopamine-agonist resistance and tumor recurrence in prolactinomas

Lower PRDM2 expression is associated with dopamine-agonist resistance and tumor recurrence in prolactinomas

10 25 1

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

13 20 3