tengfei-emory / QuantNormLinks
Mitigating the adverse impact of batch effects in sample pattern detection
☆9Updated 5 years ago
Alternatives and similar repositories for QuantNorm
Users that are interested in QuantNorm are comparing it to the libraries listed below
Sorting:
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆26Updated 8 years ago
- countsimQC - Compare characteristic features of count data sets☆27Updated 2 months ago
- ☆19Updated 7 years ago
- zero-inflated negative binomial gene expression in R☆20Updated 7 years ago
- Examples of kallisto + sleuth☆11Updated 8 years ago
- Transcript quantification import with automatic metadata detection☆68Updated last month
- Code and simulations using biologically annotated neural networks☆21Updated 3 years ago
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.☆29Updated 10 months ago
- Independent Hypothesis Weighting☆15Updated last year
- R package for Enrichment Depletion Logos (EDLogos) and String Logos☆27Updated 6 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- A small R package to make sequencing read coverage plots in R.☆38Updated 3 years ago
- The official repository of the Bioconductor 2019 Conference Workshops☆25Updated 2 years ago
- Parse TF motifs from public databases, read into R, and scan using 'rtfbs'.☆23Updated 6 years ago
- Batch Effect Correction of RNA-seq Data through Sample Distance Matrix Adjustment☆18Updated 4 years ago
- Modelling DNA methylation profiles☆23Updated 4 years ago
- Scripts and software supplement for "Gene-level differential analysis at transcript-level resolution" by Yi, Pimentel, Bray and Pachter☆19Updated 7 years ago
- 7C: Computational Chromosome Conformation Capture by Correlation of ChIP-seq at CTCF motifs☆13Updated 6 years ago
- Analysis for svaseq paper☆19Updated 10 years ago
- Various Ideas for Confounder Adjustment in Regression☆24Updated 2 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- An R package for detecting Gene-by-Environment (GxE) interaction effects on the transcriptome using Allele Specific Expression quantified…☆21Updated 3 years ago
- ☆10Updated 7 years ago
- TOP results by CONfident efFECT Sizes.☆14Updated 6 months ago
- R package for reading in & working with NucleoATAC outputs☆26Updated 6 years ago
- Code used for the single-cell RNA-Seq batch effects paper☆10Updated 7 years ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 5 years ago
- Curated Data From The Cancer Genome Atlas (TCGA) as MultiAssayExperiment Objects☆44Updated last month
- V'DJer - B Cell Receptor Repertoire Reconstruction from short read mRNA-Seq data☆29Updated 2 years ago