"Variant calling" trang 1 - tải miễn phí từ tailieunhanh
Evaluation of variant calling tools for large plant genome re-sequencing

Evaluation of variant calling tools for large plant genome re-sequencing
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CoVaCS: A consensus variant calling system

CoVaCS: A consensus variant calling system
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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
A machine learning model to determine the accuracy of variant calls in capturebased next generation sequencing

A machine learning model to determine the accuracy of variant calls in capturebased next generation sequencing
9    54    1
Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data

Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data
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ADS-HCSpark: A scalable HaplotypeCaller leveraging adaptive data segmentation to accelerate variant calling on Spark

ADS-HCSpark: A scalable HaplotypeCaller leveraging adaptive data segmentation to accelerate variant calling on Spark
13    76    1
ToTem: A tool for variant calling pipeline optimization

ToTem: A tool for variant calling pipeline optimization
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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
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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    45    1
A comparison of three variant calling pipelines using simulated data

A comparison of three variant calling pipelines using simulated data
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Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers
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Benchmarking variant identification tools for plant diversity discovery

Benchmarking variant identification tools for plant diversity discovery
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Conbase: A software for unsupervised discovery of clonal somatic mutations in single cells through read phasing

Conbase: A software for unsupervised discovery of clonal somatic mutations in single cells through read phasing
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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
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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
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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
TNER: A novel background error suppression method for mutation detection in circulating tumor DNA

TNER: A novel background error suppression method for mutation detection in circulating tumor DNA
7    65    1
Impact of post-alignment processing in variant discovery from whole exome data

Impact of post-alignment processing in variant discovery from whole exome data
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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    58    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