Proteomics Identifications & Quantitations Data Management & Integration Service
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Updated
Jan 6, 2021 - JavaScript
Proteomics Identifications & Quantitations Data Management & Integration Service
SPECifIC - Sub-Pathway ExtraCtor and enrICher
A general 16S rDNA sequencing analysis pipeline
Files needed to build and run Sequedex V2.
A workflow automation script: demultiplex the library sequence, run quality checks, deliver to archiving and processing afterwards
Lightweight library for parsing quality control information for the UMIs in 10x single cell gene expression assays
This is an R script to perform Principal Component Analysis (PCA) for High Resolution Melting (HRM) Data.
This repository contains examples of applications of deep learning on bioinformatics
This repo is a template for running differential gene expression analysis of RNA-seq count data followed by gene set enrichment analysis. This workflow is run in R using Rmarkdown. It is based around the popular R packages, DESeq2, fGSEA, and others.
Analysis of long continuous stretches of homozygosity of the human genome.
Lightweight standalone tool to reduce size of VCF files through filtering
collection of bioinformatics tools and tips, maybe | 生物信息学软件工具、分析tips集合
Genome analysis scripts and laboratory files for the UofT Bioinformatics course
An easy-to-use way for running Galaxy workflows.
summarise antiSMASH 5.0 KnownClusterBlast output
Analysis of variance (ANOVA) is a collection of statistical models and their associated estimation procedures (such as the "variation" among and between groups) used to analyze the differences among means.
Sequence Alignment tool
A curated list of awesome Bioinformatics tools.
Python code to detect ECGR Mutations; Takes a reference genome and bunch of reads as input and finds mutations (1-3 bp length) where number of supporting reads greater than 5
My solutions for the project of "An Intro to Bioinformatics" - Sharif University of Technology (SUT) - Prof. Somayyeh Koohi and Prof. Ali Sharifi-Zarchi - Fall 2021(1400-1).
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