Bioinformatic pipeline used to analyze PAS-Seq data along with instructions for use
Script associated with the bioinformatics pipeline. The first script strings the programs together (...
Next Generation Sequencing (NGS) ChIP-Seq and RNA-Seq allow systematic study of genome wide protein-...
Bioinformatic Analysis pipeLine for SomAtic Mutations In CancerIf you use this software, please cite...
Bioinformatic pipeline used to analyze PAS-Seq data along with instructions for use
A description of the bioinformatics pipeline used to process raw MiSeq data, including parameter val...
This is the artifact submitted alongside the Seq paper to OOPSLA 2019, which consists of a VM contai...
<p>Laboratory pipeline for simultaneous depletion of rRNA from prokaryotic and eukaryotic RNA mixtur...
The file contains all the commandds used in this study to generate the final data. The bioinformatic...
<p>Transcriptome de(upper left), RNA-seqresult mapping and bioinformatic analysis of the transcripto...
QMAP-Seq code for converting fastq files into relative cell numbers, plotting dose-response curves, ...
RNA-seq libraries used for transcript discovery and alternative splicing analysi
Nextflow pipeline for RNA-seq data processing developed by the Curie Bioinformatics Core facility. s...
Bioinformatics code for assembling transcriptomes, mapping reads, clustering gene families, performi...
<p>RNA-seq data analysis pipelines for (A) variant calling and filtering to detect point mutations, ...
Nextflow pipeline for RNA-seq data processing developed by the Curie Bioinformatics Core facility. s...
Script associated with the bioinformatics pipeline. The first script strings the programs together (...
Next Generation Sequencing (NGS) ChIP-Seq and RNA-Seq allow systematic study of genome wide protein-...
Bioinformatic Analysis pipeLine for SomAtic Mutations In CancerIf you use this software, please cite...
Bioinformatic pipeline used to analyze PAS-Seq data along with instructions for use
A description of the bioinformatics pipeline used to process raw MiSeq data, including parameter val...
This is the artifact submitted alongside the Seq paper to OOPSLA 2019, which consists of a VM contai...
<p>Laboratory pipeline for simultaneous depletion of rRNA from prokaryotic and eukaryotic RNA mixtur...
The file contains all the commandds used in this study to generate the final data. The bioinformatic...
<p>Transcriptome de(upper left), RNA-seqresult mapping and bioinformatic analysis of the transcripto...
QMAP-Seq code for converting fastq files into relative cell numbers, plotting dose-response curves, ...
RNA-seq libraries used for transcript discovery and alternative splicing analysi
Nextflow pipeline for RNA-seq data processing developed by the Curie Bioinformatics Core facility. s...
Bioinformatics code for assembling transcriptomes, mapping reads, clustering gene families, performi...
<p>RNA-seq data analysis pipelines for (A) variant calling and filtering to detect point mutations, ...
Nextflow pipeline for RNA-seq data processing developed by the Curie Bioinformatics Core facility. s...
Script associated with the bioinformatics pipeline. The first script strings the programs together (...
Next Generation Sequencing (NGS) ChIP-Seq and RNA-Seq allow systematic study of genome wide protein-...
Bioinformatic Analysis pipeLine for SomAtic Mutations In CancerIf you use this software, please cite...