"variant prioritisation" trang 11 - tải miễn phí từ tailieuXANH
COP1, the negative regulator of ETV1, influences prognosis in triple-negative breast cancer

COP1, the negative regulator of ETV1, influences prognosis in triple-negative breast cancer
10    56    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    45    0
Little evidence for association between the TGFBR1*6A variant and colorectal cancer: A familybased association study on non-syndromic family members from Australia and Spain

Little evidence for association between the TGFBR1*6A variant and colorectal cancer: A familybased association study on non-syndromic family members from Australia and Spain
8    51    0
Functional promoter -31G/C variant of Survivin gene predict prostate cancer susceptibility among Chinese: A case control study

Functional promoter -31G/C variant of Survivin gene predict prostate cancer susceptibility among Chinese: A case control study
7    78    0
Expression of a LINE-1 endonuclease variant in gastric cancer: Its association with clinicopathological parameters

Expression of a LINE-1 endonuclease variant in gastric cancer: Its association with clinicopathological parameters
9    63    0
A pri-miR-218 variant and risk of cervical carcinoma in Chinese women

A pri-miR-218 variant and risk of cervical carcinoma in Chinese women
8    72    0
A rare case of primary clear cell sarcoma of the pubic bone resembling small round cell tumor: An unusual morphological variant

A rare case of primary clear cell sarcoma of the pubic bone resembling small round cell tumor: An unusual morphological variant
4    56    0
GeDi: Applying suffix arrays to increase the repertoire of detectable SNVs in tumour genomes

GeDi: Applying suffix arrays to increase the repertoire of detectable SNVs in tumour genomes
12    68    0
A novel virtual barcode strategy for accurate panel-wide variant calling in circulating tumor DNA

A novel virtual barcode strategy for accurate panel-wide variant calling in circulating tumor DNA
13    100    0
NucBreak: Location of structural errors in a genome assembly by using paired-end Illumina reads

NucBreak: Location of structural errors in a genome assembly by using paired-end Illumina reads
11    50    0
MoMI-G: Modular multi-scale integrated genome graph browser

MoMI-G: Modular multi-scale integrated genome graph browser
14    61    0
DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

DNAscan: Personal computer compatible NGS analysis, annotation and visualisation
10    53    0
VIST - a Variant-Information search tool for precision oncology

VIST - a Variant-Information search tool for precision oncology
11    65    0
DeepPVP: Phenotype-based prioritization of causative variants using deep learning

DeepPVP: Phenotype-based prioritization of causative variants using deep learning
8    79    0
SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization
4    72    0
Comparing the performance of selected variant callers using synthetic data and genome segmentation

Comparing the performance of selected variant callers using synthetic data and genome segmentation
11    52    0
VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database

VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database
14    66    0
MutScan: Fast detection and visualization of target mutations by scanning FASTQ data

MutScan: Fast detection and visualization of target mutations by scanning FASTQ data
11    49    0
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    49    0
Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection
9    49    0
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