Name: Abdoallah Sharaf
Type: User
Bio: Presently, I'm a senior bioinformatician at SequAna - Sequencing Analysis Core Facility, University of Konstanz
Twitter: abdo_3a
Location: SequAna - Sequencing Analysis Core Facility, University of Konstanz
Blog: https://abdosha.wixsite.com/asharaf
Abdoallah Sharaf's Projects
Course material for the 2020-07-machine-learning course at SIB
High throughput protein function annotation with Human Readable Description (HRDs) and Gene Ontology (GO) Terms.
Algorithm for secondary de novo genome assembly guided by closely related references
An implementation of the DeepMind's AlphaFold based on PyTorch for research
A clone of the official AMOS git repo on sourceforge: https://sourceforge.net/projects/amos/
Annocript is a pipeline for the annotation of de-novo generated transcriptomes. It executes BLAST analysis with UniProt, NCBI Conserved Domain Database and Nucleotide divisions, Gene Ontology, UniPathways and the Enzyme Commission. It gives information about the longest ORF (using DNA2PEP) and non-coding potential of the sequences (using Portrait). A final heuristic makes Annocript able to identify putative long non-coding RNAs among your transcripts. Like our facebook page to be always updated: https://www.facebook.com/annocript
Applied Computational Genomics Course at UU: Spring 2018
ATLAS - Three commands to start analysing your metagenome data
Genome annotation with AUGUSTUS
(Not Offical) BBMap short read aligner, and other bioinformatic tools.
Bacterial Isolate Genome Sequence Database
BioVirusHost: A simple Python interface to query the information from Virus-Host DB
Bioinformatics Tools
Modular command-line solution for visualisation, quality control and taxonomic partitioning of genome datasets
Redesigning BlobTools to support interactive data exploration
Analyze changes in gene family size and provide a statistical foundation for evolutionary inferences.
A single molecule sequence assembler for genomes large and small.
Script for extracting Coding DNA Sequence (CDS) values from a GB file.
Combined visualisation of phylogenetic and sequence data. Please see 'release' tab for executables and documentation below
CloudBioLinux: configure virtual (or real) machines with tools for biological analyses
For all your cluster needs
Scripts and steps for making a consolidated COG database file for tools like DIAMOND.
A genome completeness evaluation tool based on miniprot
Make Complex Heatmaps