-
Seoul National University
- South Korea, Seoul
-
15:49
(UTC +09:00) - https://biosci.snu.ac.kr/limsfep/people/current?mode=view&memidx=1297
- https://orcid.org/my-orcid?orcid=0000-0002-5948-1836
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rattler-build is a universal package builder for Windows, macOS and Linux
Implementation of Alphafold 3 in Pytorch
Extracting Tables from Document Images using a Multi-stage Pipeline for Table Detection and Table Structure Recognition:
Determine presence of telomeres and visualise genome assembly scaffolds.
Turn (almost) any Python command line program into a full GUI application with one line
RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences.
Simple perl scripts for dealing with infernal and/or hmmer output/input.
This package contains deep learning models and related scripts for RoseTTAFold
Reinforcement learning for improving components in fungal BGCs
A logistic regression model for testing differential abundance in compositional microbiome data
A comparative genomics workflow using Nextflow, conda, Julia and R
kblin / python-mibig
Forked from mibig-secmet/python-mibigPython handling of MIBiG data
Supervised learning on phylogeneticallydistributed data
Universal and efficient core gene phylogeny with Foldseek and ProstT5
A telomere-to-telomere toolkit for gap-free genome assembly and centromeric repeat identification
Evolutionary Scale Modeling (esm): Pretrained language models for proteins
BGC Detection and Classification Using Deep Learning
Software that separates very close sequences that have been collapsed during assembly. Uses only long reads.
Minimizer-based assembly scaffolding and mapping using long reads
HaploKit / HyLight
Forked from kangxiongbin/HyLightHyLight is a strain aware de novo assembly method based on the overlap-layout-consensus (OLC) paradigm that leverages the strengths of NGS and 3rd generation sequencing to rapidly and accurately as…
CrossHyLight is a strain aware de novo assembly method based on the overlap-layout-consensus (OLC) paradigm that leverages the strengths of NGS and 3rd generation sequencing to rapidly and accurate…
A statistical framework for ploidy estimation using NGS short-read data
A tool for representing genomic potential and transcriptomic expression into KEGG pathways