"variant prioritization" trang 12 - tải miễn phí từ tailieunhanh
MoMI-G: Modular multi-scale integrated genome graph browser

MoMI-G: Modular multi-scale integrated genome graph browser
14    49    1
DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

DNAscan: Personal computer compatible NGS analysis, annotation and visualisation
10    62    1
VIST - a Variant-Information search tool for precision oncology

VIST - a Variant-Information search tool for precision oncology
11    41    1
DeepPVP: Phenotype-based prioritization of causative variants using deep learning

DeepPVP: Phenotype-based prioritization of causative variants using deep learning
8    35    1
SV-Pop: Population-based structural variant analysis and visualization

SV-Pop: Population-based structural variant analysis and visualization
4    58    1
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    62    1
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    43    1
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    76    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
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    57    1
A study on fast calling variants from nextgeneration sequencing data using decision tree

A study on fast calling variants from nextgeneration sequencing data using decision tree
14    63    1
Detecting large deletions at base pair level by combining split read and paired read data

Detecting large deletions at base pair level by combining split read and paired read data
7    70    1
Canary: An atomic pipeline for clinical amplicon assays

Canary: An atomic pipeline for clinical amplicon assays
7    60    1
Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform

Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform
10    76    1
A comparison of genotyping-by-sequencing analysis methods on low-coverage crop datasets shows advantages of a new workflow, GB-eaSy

A comparison of genotyping-by-sequencing analysis methods on low-coverage crop datasets shows advantages of a new workflow, GB-eaSy
12    46    1
High-throughput PCR assay design for targeted resequencing using primerXL

High-throughput PCR assay design for targeted resequencing using primerXL
9    68    1
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome

An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome
8    63    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
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
JACUSA: Site-specific identification of RNA editing events from replicate sequencing data

JACUSA: Site-specific identification of RNA editing events from replicate sequencing data
15    37    1