An open API service indexing awesome lists of open source software.

Projects in Awesome Lists by VCCRI

A curated list of projects in awesome lists by VCCRI .

https://github.com/vccri/cidr

Clustering through Imputation and Dimensionality Reduction

Last synced: 10 Apr 2025

https://github.com/vccri/sierra

Discover differential transcript usage from polyA-captured single cell RNA-seq data

alternative-polyadenylation alternative-splicing isoforms scrna-seq sierra

Last synced: 10 Apr 2025

https://github.com/vccri/falco

A quick and flexible single-cell RNA-seq processing framework on the cloud

Last synced: 10 Apr 2025

https://github.com/VCCRI/Falco

A quick and flexible single-cell RNA-seq processing framework on the cloud

Last synced: 08 Apr 2025

https://github.com/vccri/svpv

Structural Variant Prediction Viewer

Last synced: 10 Apr 2025

https://github.com/vccri/ularcirc

An R-shiny app that provides backsplice and canonical splicing analysis for both circular RNA (circRNA) and parental transcripts

backsplicing circrna circular-rna rna-seq rna-seq-analysis sequencing-rna splicing-analyses splicing-visualization

Last synced: 10 Apr 2025

https://github.com/vccri/cardiacprofiler

CardiacProfileR: An R package for extraction and visualisation of heart rate profiles from wearable fitness trackers

Last synced: 10 Apr 2025

https://github.com/vccri/vpot

VPOT - Variant Prioritisation Ordering Tool. VPOT is a Python tool written to allow prioritisation of variants in ANNOVAR annotated VCF files.

predictor prioritisation variants

Last synced: 10 Apr 2025

https://github.com/vccri/flowgrid

Last synced: 10 Apr 2025

https://github.com/vccri/dv-trio

dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCFs) created by DeepVariants are then co_called together using GATK[2]. The resultant trio VCF is then post-processing with FamSeq[3] to eliminate mendelian errors.

father-mother-child mendelian-genetics variant-calling variants

Last synced: 10 Apr 2025

https://github.com/vccri/xgsa

XGSA: a statistical method for cross-species gene set analysis

Last synced: 10 Apr 2025

https://github.com/vccri/hactive

Last synced: 10 Apr 2025

https://github.com/vccri/cidr-examples

Examples relating to the CIDR package.

Last synced: 10 Apr 2025

https://github.com/vccri/georacle

Last synced: 10 Apr 2025

https://github.com/vccri/starmap

Immersive three dimensional visualisation of single cell data using smartphone-enabled virtual reality

Last synced: 10 Apr 2025

https://github.com/vccri/sctalk

Intercellular communication analysis for scRNA-seq data

intercellular-communication ligand-receptor scrna-seq scrna-seq-analysis

Last synced: 10 Apr 2025

https://github.com/vccri/conanvarvar

ConanVarvar: a versatile tool for the detection of large syndromic copy number variation from whole genome sequencing data

bioinformatics copy-number-variation genomics

Last synced: 10 Apr 2025

https://github.com/vccri/scavenger

A pipeline for recovery of unaligned reads utilising similarity with aligned reads

Last synced: 10 Apr 2025

https://github.com/vccri/pbrowse

A real-time collaborative genome browser

Last synced: 10 Apr 2025

https://github.com/vccri/spliceogen

Last synced: 10 Apr 2025

https://github.com/vccri/atlantool

Command line tool to index and search BAM files by QNAME

Last synced: 10 Apr 2025

https://github.com/vccri/fibroblastintegration

Code related to the integration analysis of cardiac fibroblasts

Last synced: 28 Mar 2025

https://github.com/vccri/georacleplus

Last synced: 28 Mar 2025

https://github.com/vccri/spagi

Signalling Pathway Analysis for putative Gene regulatory network Identification

Last synced: 10 Apr 2025

https://github.com/vccri/cardiac-image-analysis

Images, macros and analysis pipelines for the quantitative analysis of cardiac parameters from microscopy images

Last synced: 28 Mar 2025

https://github.com/vccri/scluster

Sparse supervised clustering

Last synced: 28 Mar 2025

https://github.com/vccri/jointsv

Last synced: 28 Mar 2025

https://github.com/vccri/pad

PAD (Proximal and Distal) clustering

Last synced: 28 Mar 2025

https://github.com/vccri/ssnvs

Last synced: 28 Mar 2025

https://github.com/vccri/c3

C3: An R package for cross-species compendium-based cell-type identification

Last synced: 28 Mar 2025

https://github.com/vccri/kica

KICA: A MATLAB package for high-throughput analysis of calcium and voltage imaging data from cardiac cells

Last synced: 09 Apr 2025

https://github.com/vccri/seqvis

Last synced: 28 Mar 2025

https://github.com/vccri/caps

Last synced: 28 Mar 2025

https://github.com/vccri/ecological_study_asbestos_ard_2022

A 2022 ecological study of asbestos consumption and asbestos related diseases (ARD)

Last synced: 28 Mar 2025

https://github.com/vccri/vscode-devcontainer-dockerfile

Initiate a VS Code dev container from a dockerfile

devcontainer development devops docker dockerfile

Last synced: 16 Mar 2025

https://github.com/vccri/dcm_polygenic_study_2024

A 2024 study on polygenic risk scores and familial inheritance of dilated cardiomyopathy

Last synced: 28 Mar 2025

https://github.com/vccri/lqts-bb-hons24

LQTS BB Honours Project 2024 (itak1): Holter feature detection, heatmap and paired analysis of Holter ECGs

Last synced: 28 Mar 2025

https://github.com/vccri/cmmolecularsignatures

Cardiomyocyte molecular signatures

Last synced: 28 Mar 2025

https://github.com/vccri/from_dels_to_retrogenes

Identify retrocopied genes from whole genome sequencing structural variant clean intron deletions

Last synced: 28 Mar 2025

https://github.com/vccri/splicesm

Last synced: 28 Mar 2025

https://github.com/vccri/companyportal

Company-Portal-Icon

Last synced: 28 Mar 2025

https://github.com/vccri/variant_calling_and_annotation_pipeline

Scripts to call, annotate and analyse variants for multiple samples of whole genome sequencing (WGS)

Last synced: 28 Mar 2025

https://github.com/vccri/owl

Automated Denoising Application utilising ITV Algorithm and Image Registration

Last synced: 28 Mar 2025

https://github.com/vccri/triosim

Last synced: 28 Mar 2025

https://github.com/vccri/metadenovo

MetaDenovo : An automated framework to detect de novo mutations from whole genome trio data using cloud computing technology.

Last synced: 28 Mar 2025