"Calling for help" 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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Comparing a few SNP calling algorithms using low-coverage sequencing data

Comparing a few SNP calling algorithms using low-coverage sequencing data
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FitTetra 2.0 – improved genotype calling for tetraploids with multiple population and parental data support

FitTetra 2.0 – improved genotype calling for tetraploids with multiple population and parental data support
8    34    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
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EGL Calling Java

EGL Calling Java
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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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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
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ToTem: A tool for variant calling pipeline optimization

ToTem: A tool for variant calling pipeline optimization
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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
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A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data
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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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Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm

Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm
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Biological relevance of CNV calling methods using familial relatedness including monozygotic twins

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins
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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
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Towards pan-genome read alignment to improve variation calling

Towards pan-genome read alignment to improve variation calling
8    60    1
CoVaCS: A consensus variant calling system

CoVaCS: A consensus variant calling system
9    39    1
MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data
11    54    1
Lecture Windows programming - Lesson 7: Calling convention

Lecture Windows programming - Lesson 7: Calling convention
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