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National Institutes of Health
- Bethesda, MD
- http://molleraj.homelinuxserver.org/oldwebsite
- @abraham_moller
Stars
tools for working with Bisulfite Sequencing data while preserving reads intrinsic dependencies
Collection of tools for the analysis of CpG data
WDL workflows for variant calling and assembly using ONT
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Basic electric control line model aircraft timer using an Adafruit Trinket M0 & CircuitPython
Workflow management system written as a pure Python package and command-line utility. It supports complex workflows modeled as directed- acyclic graphs (DAGs), and execution on batch schedulers
Pipeline for streamlined fine mapping of potentially causal QTL variants
Tools to convert Illumina IDAT/BPM/EGT/GTC and Affymetrix CEL/CHP files to VCF
Comparison of methylation calling between ONT long-read R.9 and R.10 data
NIH-CARD / CARDlongread-bioinformatics-tutorial
Forked from molleraj/CARDlongread-bioinformatics-tutorialSummarizing the foundational data management, processing, and analysis steps we do in the NIA CARD LRS group.
Tools to parse cramino QC output in bulk and generate an analytics dashboard from the bulk summary.
Firmware for 3 keyboards(QWERTY, GameBoy, Calculator). They are based on MEGA328 chip.
Scripts the CARD long read team uses to query data from the MinKNOW API
Forked CARDlongread-report-parser repository
Scripts and workflows for use analyzing UK Biobank data from the DNANexus Research Analysis Platform
Source for "The computational guide to Fiber-seq"
scikit-learn: machine learning in Python
Specifications for output files from MinKNOW, dorado and others
A Snakemake workflow for calling Fiber-seq Inferred Regulatory Elements (FIREs) on single molecules.
Scripts and guidelines for standard benchmarking of methylation calling in Oxford Nanopore (ONT) long read sequencing data
Code repository for analysis performed on NABEC/HBCC ONT WGS data release, including QTL analysis workflows.
Single-cell multiome processing pipeline with downstream analysis modules
Repository for the allele-specifc QTL pipeline developed by the CARD long-read sequencing/applied neurogenomics group.
A *fast* tool for BAM/CRAM quality evaluation, intended for long reads