"Generation sequencing" trang 1 - tải miễn phí từ tailieunhanh
PaSS: A sequencing simulator for PacBio sequencing

PaSS: A sequencing simulator for PacBio sequencing
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The applications of massive parallel sequencing (next-generation sequencing) in research and molecular diagnosis of human genetic diseases

The applications of massive parallel sequencing (next-generation sequencing) in research and molecular diagnosis of human genetic diseases
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Transcriptome analysis of banana (Musa balbisiana) based on next-generation sequencing technology

Transcriptome analysis of banana (Musa balbisiana) based on next-generation sequencing technology
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Identification of differentially expressed microRNAs in primary esophageal achalasia by next-generation sequencing

Identification of differentially expressed microRNAs in primary esophageal achalasia by next-generation sequencing
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Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients

Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients
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SMOOTH-seq: Single-cell genome sequencing of human cells on a thirdgeneration sequencing platform

SMOOTH-seq: Single-cell genome sequencing of human cells on a thirdgeneration sequencing platform
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Comparison of high resolution melting analysis, pyrosequencing, next generation sequencing and immunohistochemistry to conventional Sanger sequencing for the detection of p.V600E and non-p.V600E BRAF mutations

Comparison of high resolution melting analysis, pyrosequencing, next generation sequencing and immunohistochemistry to conventional Sanger sequencing for the detection of p.V600E and non-p.V600E BRAF mutations
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SequelTools: A suite of tools for working with PacBio Sequel raw sequence data

SequelTools: A suite of tools for working with PacBio Sequel raw sequence 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
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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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Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data

Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data
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Benchmarking of computational errorcorrection methods for next-generation sequencing data

Benchmarking of computational errorcorrection methods for next-generation sequencing data
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A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing
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HGT-ID: An efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data

HGT-ID: An efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data
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Rapid evaluation and quality control of next generation sequencing data with FaQCs

Rapid evaluation and quality control of next generation sequencing data with FaQCs
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ANGSD: Analysis of next generation sequencing data

ANGSD: Analysis of next generation sequencing data
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Adaptation of Oxford Nanopore technology for hepatitis C whole genome sequencing and identification of within-host viral variants

Adaptation of Oxford Nanopore technology for hepatitis C whole genome sequencing and identification of within-host viral variants
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The real cost of sequencing: Scaling computation to keep pace with data generation

The real cost of sequencing: Scaling computation to keep pace with data generation
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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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Enrichment post-library preparation enhances the sensitivity of highthroughput sequencing-based detection and characterization of viruses from complex samples

Enrichment post-library preparation enhances the sensitivity of highthroughput sequencing-based detection and characterization of viruses from complex samples
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