Jordan Eizenga (jeizenga)

jeizenga

Geek Repo

Company:University of California Santa Cruz Genomics Institute

Location:Los Angeles, CA

Home Page:https://scholar.google.com/citations?user=rWNHPpAAAAAJ&hl=en&oi=ao

Twitter:@jeizenga

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Jordan Eizenga's repositories

wfalm

Refinements of the WFA alignment algorithm with better complexity

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centrolign

Multiple sequence alignment of long tandem repeats

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SeqPrep2

Tool for stripping adaptors and/or merging paired reads with overlap into single reads.

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structures

A collection of c++ data structures I've coded up for various projects

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hdp_mixture

Hierarchical Dirichlet process mixture model

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vg

tools for working with variation graphs

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cwl-intro-gui-workshop

Materials to teach workshop about CWL using the Rabix Composer

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gbwt

Substring index for paths in a graph

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gbwtgraph

GBWT-based handle graph

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gcsa2

BWT-based index for graphs

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genome-stratifications

Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium. These files can be used as standard resource of BED files for use with GA4GH benchmarking tools such as hap.py to stratify true positive, false positive, and false negative variant calls based on genomic context.

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gssw

efficient alignment of strings to partially ordered string graphs

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mmmultimap

memory mapped multimap based on an in-place parallel binary sort and succinct indexes

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mummer

Mummer alignment tool

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odgi

optimized dynamic genome graph implementation

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phantompeakqualtools

This package computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to obtain robust estimates of the predominant fragment length or characteristic tag shift values in these assays.

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rpvg

Method for inferring path posterior probabilities and abundances from pangenome graph read alignments

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scikit-learn

scikit-learn: machine learning in Python

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sglib

Optimized sequence graph implementations for graph genomics

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shasta

Experimental software for de novo assembly from Nanopore sequencing data.

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Ukkonen-SuffixTree

A C++ implementation of a Generalized Suffix Tree using Ukkonen's algorithm

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vgrna-project-scripts

Scripts used in vgrna project

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whatshap

Read-based phasing of genomic variants, also called haplotype assembly

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xg

succinct labeled graphs with collections and paths

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xg-1

xg0: a simpler xg index

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