Adam Taranto

Login: Adamtaranto

Company: The Australian National University

Location: Canberra, Australia

Bio: null

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Repositories

2016-01-21-training-prep
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bioconda-recipes
Conda recipes for the bioconda channel.
blast-besties
Rapid discovery of reciprocal best blast pairs.
catcount
Concatenate count tables for RNA-seq reads mapped to features by htseq-count
Corset-tools
Companion scripts for annotation of Corset generated transcript clusters.
density-Mapr
An R workflow for creating heat-maps representing the spatial association between two genomic feature sets
deRIP2
Predict progenitor sequence of fungal repeat families by correcting for RIP-like mutations and cytosine deamination events.
flo
Transfer annotations between genome assemblies using chained whole-genome alignment and UCSC LiftOver. Forked from wurmlab/flo.
frisk
Screen genomic scaffolds for regions of unusual k-mer composition.
gi2descript
Fetch summary data from NCBI for genbank records using GI numbers
hmmlearn
Hidden Markov Models in Python, with scikit-learn like API
HowToScience
A knowledge engine for new students of bioinformatics.
jcvi
Python utility libraries on genome assembly, annotation and comparative genomics
LTR-Harvest-Reformat
Correct sequence names in LTR_Harvest GFF3 output.
methFreq
Calculate observed vs expected instances of DNA-methylation motifs in gene sequences
mimeo
Scan genomes for internally repeated sequences, elements which are repetitive in another species, or high-identity HGT candidate regions between species.
MITE_Hunter_2
Minor edits to allow MITE_Hunter (Han & Wessler 2010) to use modern blast+
mpg
Markovian sequence generator
nearestfeat
Fork of nearestfeat, a tool for calculating distance between members of feature classes in a GFF annotation. Migrating to Python3
promer2circos
Takes promer sequence matches formatted with show_coords, and reformats for use as a circos linkage track
pymummer
Python3 module for running MUMmer and reading the output
quick-ortho-fetch
Take an XML formatted multiblast result, extract genbank IDs for best x hits to each query and download a non-redundant list of matching seqs from ncbi.
RECONcile
Take clustered element fragment coordinates from RECON and write sequences to fasta for alignment and consensus calling.
Ribbon
Long read visualizer for genomics created using D3
sickle_team8
Giving a go at sickle
subset-fasta-by-name
Subset, split, and correct formatting of multiple sequence FASTA files.
SWC_ANU_2016
Python Stuff
TE-Annotation-Workflow
Workflow and useful tools for annotating transposable elements in sequenced genomes
TE-dispersion-metric
Proposed metric for measuring the clustering of transposons within a genome
TE-insertion-scanner
Scan whole genome alignments for signatures of transposon insertion.
TE-Reunite
For a set of reference transposons, collect instances from one or more genomes. Use aligned collections to build models capturing TE family diversity or produce deRIP'd reference sequence.
TE-splitter
Extract terminal repeats from retrotransposons (LTRs) or DNA transposons (TIRs). Compose synthetic MITES from complete DNA transposons.
TIRmite
Map TIR-pHMM models to genomic sequences for annotation of MITES and complete DNA-Transposons.
Transposon-Tools-List
A list of useful software tools for predicting, classifying, annotating, and analysing Transposable Elements.
TRF2GFF
Convert Tandem Repeat Finder dat file output into gff3 format
Yanagiba
Filter and slice Nanopore reads which have been basecalled with Albacore.

Commits To

RepositoryMost Recent Commit# Commits
ISA-tools/bioconda-recipes2017-10-24 18:11:29.04


This work is supported by the National Institutes of Health's National Center for Advancing Translational Sciences, Grant Number U24TR002306. This work is solely the responsibility of the creators and does not necessarily represent the official views of the National Institutes of Health.