"variant priorization" trang 3 - tải miễn phí từ tailieuXANH
Impact of post-alignment processing in variant discovery from whole exome data

Impact of post-alignment processing in variant discovery from whole exome data
13    68    0
TarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine

TarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine
13    96    0
Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles

Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles
8    126    0
A hybrid computational strategy to address WGS variant analysis in >5000 samples

A hybrid computational strategy to address WGS variant analysis in >5000 samples
12    66    0
Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies

Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies
14    55    0
Feature selection algorithm based on dual correlation filters for cancer‑associated somatic variants

Feature selection algorithm based on dual correlation filters for cancer‑associated somatic variants
19    90    0
Comparing variant calling algorithms for target-exon sequencing in a large sample

Comparing variant calling algorithms for target-exon sequencing in a large sample
10    54    0
A novel p.A191D matrilin-3 variant in a Vietnamese family with multiple epiphyseal dysplasia: A case report

A novel p.A191D matrilin-3 variant in a Vietnamese family with multiple epiphyseal dysplasia: A case report
8    50    0
Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: Sibling case report and literature review

Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: Sibling case report and literature review
11    38    1
Small airway dysfunction in patients with cough variant asthma: A retrospective cohort study

Small airway dysfunction in patients with cough variant asthma: A retrospective cohort study
8    38    1
Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants

Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants
9    31    1
Towards a better understanding of the low recall of insertion variants with short-read based variant callers

Towards a better understanding of the low recall of insertion variants with short-read based variant callers
17    80    1
Benchmarking subcellular localization and variant tolerance predictors on membrane proteins

Benchmarking subcellular localization and variant tolerance predictors on membrane proteins
15    127    1
RADAR: Annotation and prioritization of variants in the post-transcriptional regulome of RNA-binding proteins

RADAR: Annotation and prioritization of variants in the post-transcriptional regulome of RNA-binding proteins
13    225    1
PRINCESS: Comprehensive detection of haplotype resolved SNVs, SVs, and methylation

PRINCESS: Comprehensive detection of haplotype resolved SNVs, SVs, and methylation
17    141    1
Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery

Bovine breed-specific augmented reference graphs facilitate accurate sequence read mapping and unbiased variant discovery
27    188    1
PSCAN: Spatial scan tests guided by protein structures improve complex disease gene discovery and signal variant detection

PSCAN: Spatial scan tests guided by protein structures improve complex disease gene discovery and signal variant detection
25    82    1
The Ensembl variant effect predictor

The Ensembl variant effect predictor
14    178    1
Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines

Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines
12    160    2
GAVIN: Gene-Aware Variant INterpretation for medical sequencing

GAVIN: Gene-Aware Variant INterpretation for medical sequencing
10    218    2
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.