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This project assembles short sequencing reads into contigs using a greedy overlap algorithm and computes coverage across merged contigs. It also performs ORF detection using motif scoring, start/stop codons, and outputs annotated ORFs in FASTA format.
MucOneUp simulates diploid MUC1 VNTR references with variable repeats, targeted mutations, and toxic protein detection. It also integrates an Illumina read simulation pipeline for comprehensive genomic benchmarking.
This repository empowers you to perform operations such as generating complementary sequences, translating DNA to RNA, and identifying open reading frames (ORFs) with ease. Also DNA-to Protein and Protein-to DNA
This repository contains scripts used to clean genome sequencing data; such that it passes quality control for analysis. Script(s) include: Open Reading Frame. Code is written in Python 3. Spring 2021
Computational programs and algorithms used to convert information from biochemical experiments (DNA/RNA/Protein/DNA chip/NGS) into useful information and data.
This code is not working perfectly as it prints out the incorrect frame numbers. However it is a good starting point for anyone doing a project. Feel free to fork or commit.