slowkow

:round_pushpin: Repel overlapping text labels away from each other in your ggplot2 figures.

📚 Tools and databases for analyzing HLA and VDJ genes.

🎼 Integrate multiple high-dimensional datasets with fuzzy k-means and locally linear adjustments.

:snake: Snakefiles for common RNA-seq data analysis workflows (STAR and Kallisto).

:card_index: Retrieve data in genomic intervals with a Python interface for tabix.

:dart: Human transcription factor target genes from 6 databases in convenient R format.

:vertical_traffic_light: Run Picard on BAM files and collate 90 metrics into one file.

:bar_chart: Identify cell types and pathways affected by genetic risk loci.

:bookmark: Get SNP proxies from the 1000 Genomes Project.

:bug: How to use CENTIPEDE to determine if a transcription factor is bound.

🧭 Navigate single-cell RNA-seq datasets in your web browser.

Read HOMER motif analysis output in R.

:orange_book: Explore 1000 Genomes variant data with JavaScript.

Kamil's dotfiles