"sequencing simulator" trang 3 - tải miễn phí từ tailieuXANH
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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SCOPIT: Sample size calculations for singlecell sequencing experiments

SCOPIT: Sample size calculations for singlecell sequencing experiments
6    65    0
Learning mutational graphs of individual tumour evolution from single-cell and multi-region sequencing data

Learning mutational graphs of individual tumour evolution from single-cell and multi-region sequencing data
13    58    0
Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets

Quantification of experimentally induced nucleotide conversions in high-throughput sequencing datasets
16    49    0
SEQprocess: A modularized and customizable pipeline framework for NGS processing in R package

SEQprocess: A modularized and customizable pipeline framework for NGS processing in R package
7    75    0
DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data
10    57    0
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    68    0
MERIT reveals the impact of genomic context on sequencing error rate in ultra-deep applications

MERIT reveals the impact of genomic context on sequencing error rate in ultra-deep applications
13    90    0
16SPIP: A comprehensive analysis pipeline for rapid pathogen detection in clinical samples based on 16S metagenomic sequencing

16SPIP: A comprehensive analysis pipeline for rapid pathogen detection in clinical samples based on 16S metagenomic sequencing
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MPD: Multiplex primer design for nextgeneration targeted sequencing

MPD: Multiplex primer design for nextgeneration targeted sequencing
5    75    0
Statistical method to compare massive parallel sequencing pipelines

Statistical method to compare massive parallel sequencing pipelines
11    62    0
A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data
13    62    0
Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data

Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data
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Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells

Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
16    62    0
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    96    0
SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis

SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis
4    88    0
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    55    0
Natrix: A Snakemake‑based workfow for processing, clustering, and taxonomically assigning amplicon sequencing reads

Natrix: A Snakemake‑based workfow for processing, clustering, and taxonomically assigning amplicon sequencing reads
14    56    0
Using single cell sequencing data to model the evolutionary history of a tumor

Using single cell sequencing data to model the evolutionary history of a tumor
13    75    0
QTrim: A novel tool for the quality trimming of sequence reads generated using the Roche/454 sequencing platform

QTrim: A novel tool for the quality trimming of sequence reads generated using the Roche/454 sequencing platform
6    56    0
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