calling trang 1 tải miễn phí từ TAILIEUCHUNG

"calling" trang 1 - tải miễn phí từ Tailieuchung

Evaluation of variant calling tools for large plant genome re-sequencing

Evaluation of variant calling tools for large plant genome re-sequencing

16 48 1

Comparing a few SNP calling algorithms using low-coverage sequencing data

Comparing a few SNP calling algorithms using low-coverage sequencing data

15 19 1

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 27 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

12 26 1

EGL Calling Java

EGL Calling Java

45 62 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 33 1

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 53 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

11 46 1

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 61 1

ToTem: A tool for variant calling pipeline optimization

ToTem: A tool for variant calling pipeline optimization

9 31 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 50 1

A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data

13 29 1

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

14 41 1

Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm

Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm

10 20 1

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins

8 52 1

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 31 1

Towards pan-genome read alignment to improve variation calling

Towards pan-genome read alignment to improve variation calling

8 44 1

CoVaCS: A consensus variant calling system

CoVaCS: A consensus variant calling system

9 20 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 44 1

Lecture Windows programming - Lesson 7: Calling convention

Lecture Windows programming - Lesson 7: Calling convention

47 15 1

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