NanostrIng MB cLassifiEr
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Updated
Apr 25, 2017 - R
NanostrIng MB cLassifiEr
Fuzzy fusion finder for next generation sequencing data.
bcftools singularity container
Pipeline for bulk tissue cell-type deconvolution using single-cell RNA-seq as reference
Tool for soft-clipping PCR primers based on alignment location
amazon aws batch implementation of nextflow/rnaseq-encode-nf tutorial
Reports frequency of all single nucleotide changes for a group of fastq files
Collection of programs/scripts written for performing miscellaneous analysis on data from next generation sequencing
Deployed NGS algorithm, Disease prediction from genes and bioactivity prediction of renin in python
Genomics Commons
Removes PCR duplication from amplicon datasets
Tool for realigning soft-clipped bases from amplicon reads
Neat AWS config, workflow, pipline
Udo Stenzel's perl-ngs — a collection of Perl tools for next-generation sequencing [MIRROR]
A web platform providing accessibility to HIV NGS pipelines - Template Consensus Sequence, Drug Resistance, Outgrowth Virus Dating
BIO634 Next-Generation Sequencing 2 – Transcriptomes, Variant Calling and Biological Interpretation
Miscellaneous Bioinformatics
A web service for providing info about sequencing runs.
Create fastq symlinks for selected samples in sequencer output directories based on several criteria
Add a description, image, and links to the next-generation-sequencing topic page so that developers can more easily learn about it.
To associate your repository with the next-generation-sequencing topic, visit your repo's landing page and select "manage topics."