"Variant analysis" trang 1 - tải miễn phí từ tailieunhanh
Real world scenarios in rare variant association analysis: The impact of imbalance and sample size on the power in silico

Real world scenarios in rare variant association analysis: The impact of imbalance and sample size on the power in silico
10    56    1
OVAS: An open-source variant analysis suite with inheritance modelling

OVAS: An open-source variant analysis suite with inheritance modelling
10    55    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    13    1
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    33    1
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    67    3
Analysis on GENIE reveals novel recurrent variants that affect molecular diagnosis of sizable number of cancer patients

Analysis on GENIE reveals novel recurrent variants that affect molecular diagnosis of sizable number of cancer patients
12    46    1
PyAmpli: An amplicon-based variant filter pipeline for targeted resequencing data

PyAmpli: An amplicon-based variant filter pipeline for targeted resequencing data
6    68    1
Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles

Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles
8    45    1
MARV: A tool for genome-wide multiphenotype analysis of rare variants

MARV: A tool for genome-wide multiphenotype analysis of rare variants
8    39    1
An efficient correlation power analysis attack using variational mode decomposition

An efficient correlation power analysis attack using variational mode decomposition
8    52    3
Báo cáo khoa học: Mutational analysis of substrate recognition by human arginase type I ) agmatinase activity of the N130D variant

Báo cáo khoa học: Mutational analysis of substrate recognition by human arginase type I ) agmatinase activity of the N130D variant
7    56    0
Preliminary results on the whole genome analysis of a Vietnamese individual

Preliminary results on the whole genome analysis of a Vietnamese individual
5    99    0
Impact of KIT exon 10 M541L allelic variant on the response to imatinib in aggressive fibromatosis: Analysis of the desminib series by competitive allele specific Taqman PCR technology

Impact of KIT exon 10 M541L allelic variant on the response to imatinib in aggressive fibromatosis: Analysis of the desminib series by competitive allele specific Taqman PCR technology
8    60    1
MC-GenomeKey: A multicloud system for the detection and annotation of genomic variants

MC-GenomeKey: A multicloud system for the detection and annotation of genomic variants
14    77    1
Lecture Biomedical Signal Processing and Modeling: Analysis of Nonstationary and Multicomponent Signals - Nguyen Cong Phuong

Lecture Biomedical Signal Processing and Modeling: Analysis of Nonstationary and Multicomponent Signals - Nguyen Cong Phuong
118    60    1
On rare variants in principal component analysis of population stratification

On rare variants in principal component analysis of population stratification
11    5    1
SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization
4    58    1
GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases
6    60    1
Pan-cancer analysis of whole-genome doubling and its association with patient prognosis

Pan-cancer analysis of whole-genome doubling and its association with patient prognosis
15    1    1
Meta-analysis of Osteopontin splice variants in cancer

Meta-analysis of Osteopontin splice variants in cancer
14    6    1