Points: 272
LEGE
Walk-in Bioinformatics interview @ https:/
(65 days ago)
Skills:
About me
Discuss all about bioinformatics !
- LEGE bookmarked Virus Bioinformatics Tools
- LEGE published a blog post 16sRNA Database Download
- LEGE published a news post Cleaner BLAST Databases for More Accurate Results
- LEGE published a blog post Entire Human Genome Sequencing !
- LEGE bookmarked ExRec: Exclusion of Recombined DNA
Cleaner BLAST Databases for More Accurate Results
By LEGE 3 days agoRemoving contaminated sequences using NCBI quality assurance toolsBlast on Docker, Google Cloud, Amazon Cloud
By LEGE 1387 days agoAs announced in a previous post, we offer a Docker version of NCBI BLAST+ that you can use locally or on the Google Cloud where we have pre-loaded BLAST databases. We are happy to announce that the same functionality is now available on the...
Jit
5557 points
5557 points
Jitendra Narayan
2547 points
2547 points
Rahul Nayak
2300 points
2300 points
Neelam Jha
1578 points
1578 points
Rahul Agarwal
1188 points
1188 points
- By LEGE 65 days agoWalk-in Bioinformatics interview @ https:/
/ cdri.res.in/ pdf/ recruitment/ Advt_01_2024_Project_Staff.pdf - By LEGE 112 days ago
Python script to parse GFF file
By LEGE 29 days agoPython script to convert fastq to fasta
By LEGE 29 days agoFasta to Fastq conversion !
By LEGE 39 days agoPython script for basic stats of the assembled genome !
By LEGE 85 days ago
Virus Bioinformatics Tools
By LEGE 2 days agoevirusbioinfc.notion.site - Bioinformatics tools play a crucial role in studying viruses, enabling researchers to analyze their genetic makeup, structure, function, and evolution. Here are some commonly used bioinformatics tools for virus...Minda: a tool for evaluating structural variant (SV) callers
By LEGE 26 days agogithub.com - Minda is a tool for evaluating structural variant (SV) callers that standardizes VCF records for compatibility with both germline and somatic SV callers, benchmarks against a single VCF input file, or benchmarks against an ensemble call set...Severus: a somatic structural variation (SV) caller for long reads
By LEGE 26 days agogithub.com - Severus is a somatic structural variation (SV) caller for long reads (both PacBio and ONT). It is designed for matching tumor/normal analysis, supports multiple tumor samples, and produces accurate and complete somatic and germline calls. Severus...GraphPath: A graph attention model for molecular stratification with interpretability based on the...
By LEGE 29 days agogithub.com - Achieving accurate and interpretable clinical predictions requires paramount attention to thoroughly characterizing patients at both the molecular and biological pathway levels. In this paper, we present GraphPath, a biological knowledge-driven...
16sRNA Database Download
By LEGE 2 days agoDownloading 16S rRNA databases can be crucial for various bioinformatics analyses, especially in microbiome research.Entire Human Genome Sequencing !
By LEGE 24 days agoCost-effective whole human genome sequencing has revolutionized the landscape of genetic research and personalized medicine by making comprehensive genetic analysis accessible to a wider population. Through advancements in sequencing technologies,...Software for genome assembly !
By LEGE 1334 days agoList of bioinformatics tools/Software Website References for genome assembly:
Question: What is the p-value?
Question: Unable to restart Apache !
Question: Why bioinformatics is important ?
