Liang Ma (LiangMa2017)

LiangMa2017

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Company:UT Health San Antonio

Location:San Antonio

Home Page:https://directory.uthscsa.edu/academics/profile/mal1

Twitter:@LiangMa2017

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Liang Ma's starred repositories

rnaseq_tutorial

Informatics for RNA-seq: A web resource for analysis on the cloud. Educational tutorials and working pipelines for RNA-seq analysis including an introduction to: cloud computing, critical file formats, reference genomes, gene annotation, expression, differential expression, alternative splicing, data visualization, and interpretation.

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circlize

Circular visualization in R

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ChIP-seq-analysis

ChIP-seq analysis notes from Ming Tang

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MACS

MACS -- Model-based Analysis of ChIP-Seq

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SpliceAI

A deep learning-based tool to identify splice variants

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Intro-to-ChIPseq

Intro to ChIPseq using HPC

annotables

R data package for annotating/converting Gene IDs

chipseq_pipeline

AQUAS TF and histone ChIP-seq pipeline

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WASP

WASP: allele-specific pipeline for unbiased read mapping and molecular QTL discovery

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GeneticsMakie.jl

🧬High-performance genetics- and genomics-related data visualization using Makie.jl

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xqtl-protocol

Molecular QTL analysis protocol developed by ADSP Functional Genomics Consortium

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singlecell_neuroseq_paper

Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation

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MoSEA

Motif Scan and Enrichment Analysis (MoSEA)

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mrlocus

Older repo for MRLocus. See new website for software usage guide:

MMQTL

MMQTL is a statistical package applying meta-analysis to detect multiple QTL signals integrating signals among conditions, with control for population structure and relatedness

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cnvkit_pipeline

call copy number from WES(WXS)

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Alzheimers_DNAm

Epigenome-wide analysis of DNA methylation from Alzheimer's patients and unaffected controls

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GWAS-QC

Quality control steps for GWAS

SuRE-SNV-code

collection of repos' holding code associated with manuscript J. van Arensbergen et al: Systematic identification of human SNPs affecting regulatory element activity.

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cardips-ipsc-eqtl

CARDIPS iPSC eQTL study.

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COS_public_release

Public release of code for analysis of RNA-Seq data from COS cohort

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Hornet

Simple tools for unbiased allele-specific read mapping based on WASP by the Pritchard lab

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RNA-seq-variant-calling

Functions to call variant in RNA-Seq with Mutect2, Varscan, and Vardict

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ampad-DiffExp

Code base for performing covariate adjustments and differential expression analysis of the RNAseq data from AMP-AD.

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cisVar

cisVar scripts.

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germlinewrapper

detect germline variants from normal samples

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psychcore-compute-platform

Cloud Pipeline and Big Data Computing Platform for Bioinformatics

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Schizophrenia_CellType

Codes for Schizophrenia CellType project

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ipsdsn

Code used in the paper: "Molecular and functional variation in iPSC-derived sensory neurons"

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