"variant prioritisation" trang 12 - tải miễn phí từ tailieuXANH
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    68    0
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    45    0
Canary: An atomic pipeline for clinical amplicon assays

Canary: An atomic pipeline for clinical amplicon assays
7    52    0
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    47    0
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    56    0
High-throughput PCR assay design for targeted resequencing using primerXL

High-throughput PCR assay design for targeted resequencing using primerXL
9    62    0
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    46    0
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    66    0
MARV: A tool for genome-wide multiphenotype analysis of rare variants

MARV: A tool for genome-wide multiphenotype analysis of rare variants
8    67    0
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    62    0
GTB – an online genome tolerance browser

GTB – an online genome tolerance browser
6    63    0
An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors
7    124    0
Integrating 400 million variants from 80,000 human samples with extensive annotations: Towards a knowledge base to analyze disease cohorts

Integrating 400 million variants from 80,000 human samples with extensive annotations: Towards a knowledge base to analyze disease cohorts
13    63    0
Evaluation of variant detection software for pooled next-generation sequence data

Evaluation of variant detection software for pooled next-generation sequence data
9    64    0
Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms

Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms
14    67    0
Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline
11    86    0
Towards accurate characterization of clonal heterogeneity based on structural variation

Towards accurate characterization of clonal heterogeneity based on structural variation
12    60    0
Quantitative group testing-based overlapping pool sequencing to identify rare variant carriers

Quantitative group testing-based overlapping pool sequencing to identify rare variant carriers
14    180    0
Revitalization of heritage - The original and variant traditional integration of the het cha festival in Ang village in Moc Chau, Vietnam (study in Ang village, Moc Chau, Son La)

Revitalization of heritage - The original and variant traditional integration of the het cha festival in Ang village in Moc Chau, Vietnam (study in Ang village, Moc Chau, Son La)
11    77    0
Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing

Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing
8    53    0
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