Variant calling trang 1 tải miễn phí từ TAILIEUCHUNG

"Variant 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

CoVaCS: A consensus variant calling system

CoVaCS: A consensus variant calling system

9 20 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

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 42 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

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

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

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

15 69 1

Benchmarking variant identification tools for plant diversity discovery

Benchmarking variant identification tools for plant diversity discovery

15 21 1

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

18 7 1

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

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

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 50 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

13 58 1

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 38 1

Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles

Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles

8 33 1

Towards a better understanding of the low recall of insertion variants with short-read based variant callers

Towards a better understanding of the low recall of insertion variants with short-read based variant callers

17 15 1

Đã phát hiện trình chặn quảng cáo AdBlock

Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.