sridhar0605's Stars
Kanaries/pygwalker
PyGWalker: Turn your pandas dataframe into an interactive UI for visual analysis
man-group/dtale
Visualizer for pandas data structures
mszep/pandoc_resume
The Markdown Resume
kyclark/command-line-rust
Code for Command-Line Rust (O'Reilly, 2022, ISBN 9781098109417) https://learning.oreilly.com/library/view/command-line-rust/9781098109424/
GeostatsGuy/PythonNumericalDemos
Well-documented Python demonstrations for spatial data analytics, geostatistical and machine learning to support my courses.
moshi4/pyCirclize
Circular visualization in Python (Circos Plot, Chord Diagram, Radar Chart)
thackl/gggenomes
A grammar of graphics for comparative genomics
nstrayer/cv
My CV built using RMarkdown and the pagedown package.
Illumina/SpliceAI
A deep learning-based tool to identify splice variants
bioconvert/bioconvert
Bioconvert is a collaborative project to facilitate the interconversion of life science data from one format to another.
trevorld/ggpattern
ggplot geoms with pattern fills
dewberryants/asciiMol
Curses based ASCII molecule viewer for terminals.
wiseaidev/rust-data-analysis
Rust for data analysis encyclopedia (WIP).
genome/bam-readcount
Count bases in BAM/CRAM files
noriakis/ggkegg
Analyzing and visualizing KEGG information using the grammar of graphics
yfukasawa/LongQC
LongQC is a tool for the data quality control of the PacBio and ONT long reads.
cafferychen777/ggpicrust2
Make Picrust2 Output Analysis and Visualization Easier
mikeckennedy/umami-python
Umami Analytics Client for Python
mribeirodantas/NextflowSnippets
This repository hosts a large collection of Nextflow snippets
a-slide/NanoCount
EM based transcript abundance from nanopore reads mapped to a transcriptome with minimap2
mskilab-org/JaBbA
MIP based joint inference of copy number and rearrangement state in cancer whole genome sequence data.
adnaniazi/tailfindr
An R package for estimating poly(A)-tail lengths in Oxford Nanopore RNA and DNA reads.
Xinglab/espresso
sigven/vcf2tsvpy
Genomic VCF to tab-separated values
gaolabtools/scNanoGPS
Single cell Nanopore sequencing data for Genotype and Phenotype
NBISweden/GUESSmyLT
An efficient way to guess the library type of your RNA-Seq data.
brentp/fraguracy
overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites
srbehera/FixItFelix
tschaffter/rstudio
Docker image for analyses using RStudio and Python-Conda
seasoncloud/Clonalscope
Clonalscope is a subclone detection method based on copy number alterations (CNAs) for single-cell and ST tumor sequencing data. Clonalscope is able to detect subclones, label malignant cells, and trace subclones for both scRNA-seq and ST data.