amfrancette

biotoolbox

Tools for querying and analysis of genomic data

GrowthCurveAnalysis

Intron_Enrichment_Score

The intronic enrichment score calculates the average coverage of RNA-seq reads over introns relative to neighboring exons in Saccharomyces cerevisiae. This score can be used to quantify enrichment of nascent transcripts from techniques such as 4tU-seq and TT-seq or to quantify defects in transcript splicing.

IntronExon_Junction_Splice_Ratio

Code and associated annotation file to count the ratio of spliced an unspliced reads for all intron-containing genes.

MatchingIndex

This repository can be used to convert survey results into mentor, mentee compatibility scores.

Nucleosome_Entry_Exit_Analysis_Code

Source code for processing RNA-seq, ChIP-seq, and MNase-Seq data for Hildreth et al. "Mutations that alter the nucleosome DNA entry-exit site impair transcription termination in vivo"

RNAseq_analysis_code

This repository holds code for RNA-seq analysis handling stranded and un-stranded RNA-seq data.

SpikeinCorrectionFactor

Code related to calculating a corrective scaling factor to detect and correct for off-expecation ratios of sample to spike in for NGS experiments.

OMOPOmics

Patient 'omics data in OMOP format

birdsurvey

birdsurvey for class

amfrancette/IntronExon_Junction_Splice_Ratio

Code and associated annotation file to count the ratio of spliced an unspliced reads for all intron-containing genes.

amfrancette/biotoolbox

Tools for querying and analysis of genomic data

amfrancette/GrowthCurveAnalysis

amfrancette/Intron_Enrichment_Score

The intronic enrichment score calculates the average coverage of RNA-seq reads over introns relative to neighboring exons in Saccharomyces cerevisiae. This score can be used to quantify enrichment of nascent transcripts from techniques such as 4tU-seq and TT-seq or to quantify defects in transcript splicing.

amfrancette/MatchingIndex

This repository can be used to convert survey results into mentor, mentee compatibility scores.

amfrancette/Nucleosome_Entry_Exit_Analysis_Code

Source code for processing RNA-seq, ChIP-seq, and MNase-Seq data for Hildreth et al. "Mutations that alter the nucleosome DNA entry-exit site impair transcription termination in vivo"

amfrancette/RNAseq_analysis_code

This repository holds code for RNA-seq analysis handling stranded and un-stranded RNA-seq data.

amfrancette/SpikeinCorrectionFactor

Code related to calculating a corrective scaling factor to detect and correct for off-expecation ratios of sample to spike in for NGS experiments.