mortezasabri's Stars
yunshun/HumanBreast10X
mousepixels/sanbomics_scripts
scripts and notebooks from sanbomics
zhanghao-njmu/SCP
An end-to-end Single-Cell Pipeline designed to facilitate comprehensive analysis and exploration of single-cell data.
PASApipeline/PASApipeline
PASA software
totajuliusd/topr
topr is a collection of plotting functions for visualizing and exploring genetic association results. Association results from multiple phenotypes can be viewed simultaneously, over the entire genome (Manhattan plot) or in the more detailed regional view.
nf-core/lncpipe
UNDER DEVELOPMENT--- Analysis of long non-coding RNAs from RNA-seq datasets
artempronozin95/ICAnnoLncRNA-identification-classification-and-annotation-of-LncRNA
pachterlab/LP_2021
cxli233/Online_R_learning
Online R learning for applied statistics
ktrns/scrnaseq
Workflow for single-cell RNA-seq analysis using Seurat
OpenIntroStat/ims
📚 Introduction to Modern Statistics - A college-level open-source textbook with a modern approach highlighting multivariable relationships and simulation-based inference. For v1, see https://openintro-ims.netlify.app.
OI-Biostat/oi_biostat_labs
R labs accompanying the OpenIntro Biostatistics textbook
rogotoh/PMiFish
sarahpyfrom/PLAIDOH
Source Code for PLAIDOH LncRNA Predictive Algorithm
LeiCao97/PreLnc
A tool for predicting lncRNAs based on multiple features
emalgorithm/ncRNA-family-prediction
Code for the paper ncRNA Classification with Graph Convolutional Networks by E. Rossi et. al.
Pengeace/RPITER
A hierarchical deep learning framework for ncRNA-protein interaction prediction.
knowledgefold/gfold
This is an official replacement for https://bitbucket.org/feeldead/gfold
Gabaldonlab/lncRNAs
script of lncRNA project
SFGLab/ConsensuSV-pipeline
Automatised pipeline of ConsensuSV workflow.
bioinformatics-sannio/ncrna-deep
Scripts and datasets to reproduce the experiment of the paper "Exploring non-coding RNA functions with deep learning tools"
ursky/SnapT
Small ncRNA annotation pipeline for transcriptomics
alexcoppe/iWhale
:whale: Dockerized WES pipeline for variants identification in mathced tumor-normal samples
sjackman/abyss-activity
ABySS learning activity
bahlolab/bioinfotools
Documenting usage and experience with bioinformatic tools
tanghaibao/jcvi
Python library to facilitate genome assembly, annotation, and comparative genomics
Developer-Y/cs-video-courses
List of Computer Science courses with video lectures.
josemolina6/PaeAG1_genome
Assembly and annotation of the Pseudomonas aeruginosa AG1 genome
gencorefacility/variant-calling-pipeline-gatk4
Variant Calling Pipeline Using GATK4 and Nextflow
nf-core/sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing