"variant prioritisation" trang 4 - tải miễn phí từ tailieuXANH
Cepip: Context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes

Cepip: Context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes
15    277    2
Structural variant calling: The long and the short of it

Structural variant calling: The long and the short of it
14    154    2
Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data

Systematic comparative analysis of singlenucleotide variant detection methods from single-cell RNA sequencing data
15    88    2
Paragraph: A graph-based structural variant genotyper for short-read sequence data

Paragraph: A graph-based structural variant genotyper for short-read sequence data
13    33    2
Conbase: A software for unsupervised discovery of clonal somatic mutations in single cells through read phasing

Conbase: A software for unsupervised discovery of clonal somatic mutations in single cells through read phasing
18    17    1
Exploring experiences and needs of spousal carers of people with behavioural variant frontotemporal dementia (bvFTD) including those with familial FTD (fFTD): A qualitative study

Exploring experiences and needs of spousal carers of people with behavioural variant frontotemporal dementia (bvFTD) including those with familial FTD (fFTD): A qualitative study
11    12    1
Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa

Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa
19    13    1
Rare variant association analysis in case-parents studies by allowing for missing parental genotypes

Rare variant association analysis in case-parents studies by allowing for missing parental genotypes
8    2    1
GM2 gangliosidosis AB variant: Novel mutation from India – a case report with a review

GM2 gangliosidosis AB variant: Novel mutation from India – a case report with a review
5    42    0
The first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman’s disease

The first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman’s disease
8    58    0
Gentamicin, genetic variation and deafness in preterm children

Gentamicin, genetic variation and deafness in preterm children
4    177    0
Effective heuristics for solving dynamic variant of single processor total tardiness problems

Effective heuristics for solving dynamic variant of single processor total tardiness problems
10    42    0
Variant isoforms of CD44 involves acquisition of chemoresistance to cisplatin and has potential as a novel indicator for identifying a cisplatin-resistant population in urothelial cancer

Variant isoforms of CD44 involves acquisition of chemoresistance to cisplatin and has potential as a novel indicator for identifying a cisplatin-resistant population in urothelial cancer
11    62    0
Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites

Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites
13    68    0
Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome

Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome
8    2    1
Tài liệu cơ bản về CSS tiếng việt rất hay

Tài liệu cơ bản về CSS tiếng việt rất hay
65    109    0
Chương Sáu - Dùng dữ kiện

Chương Sáu - Dùng dữ kiện
9    32    0
Báo cáo sinh học:

Báo cáo sinh học: "Sometimes one just isn’t enough: do vertebrates contain an H2A.Z hyper-variant"
3    47    0
Báo cáo toán học:

Báo cáo toán học: "A van der Waerden Variant"
10    60    0
Báo cáo y học:

Báo cáo y học: "ribriform-Morular Variant of Papillary Carcinoma: Association with Familial Adenomatous Polyposis Report of Three Cases and Review of Literature"
7    60    0
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