BOL: Related items

SOWDHAMINI Lab

Sun, 15 Sep 2013 09:19:12 -0500

Genome sequencing projects have enormous potential for benefiting human endeavors. However, just as acquiring a language's vocabulary does not enable one to speak it, databases that list the amino acid composition of proteins do not directly tell us much about these proteins' higher-level structure and function. The most productive way to indirectly exploit these databases has been to start with the small number of proteins that are fully-characterised and to assume that other "similar" proteins will have a related structure and function. Proteins with very similar amino acid sequence are "no-brainers", but the real test, which our group largely focuses on, is to detect the "essential" similarity in proteins whose non-critical sections have experienced random rearrangements during evolution. In such cases functionally similar proteins may have less than 25% sequence overlap.

More @ http://www.ncbs.res.in/sowdhamini/groups_sowdhamini.htm

BLAST+ 5: Key Updates and Enhancements for Modern Bioinformatics

LEGE — Sat, 07 Dec 2024 22:37:48 -0600

The BLAST+ 5 (Basic Local Alignment Search Tool) update has introduced several key enhancements aimed at improving performance, user experience, and compatibility with evolving genomic data standards. Here are the major updates:

Database Enhancements:
- The BLAST databases have shifted fully to the version 5 (v5) format, which integrates built-in taxonomy information. This allows for more detailed and efficient sequence annotation and analysis.
- Protein databases in v5 are now accession-based, supporting a broader range of sequences, including those from high-throughput projects and the Pathogen Detection Project. These databases also accommodate structural proteins with multi-character chain identifiers.
Performance Improvements:
- Adaptive Composition-Based Statistics (CBS) is available as an experimental feature, enhancing the detection of novel results in protein-protein comparisons.
- Updated algorithms improve the stability of search results, especially when fewer hits are requested than the default output.
Compatibility:
- Support for the older v4 databases has been discontinued. The v5 format is now the default for all BLAST database updates, ensuring alignment with current standards in bioinformatics.
User-Friendly Changes:
- Naming conventions for databases have been simplified to enhance clarity and ease of use. For example, database names no longer include version tags like "_v5".
Future-Proofing:
- BLAST+ 5 aligns with current and upcoming data requirements, ensuring that researchers have access to the most comprehensive and modern resources for sequence alignment.

These updates reflect NCBI's commitment to maintaining BLAST as a leading tool for sequence analysis. For detailed release notes and additional guidance, refer to NCBI Insights here

16sRNA Database Download

LEGE — Wed, 24 Apr 2024 04:33:15 -0500

Downloading 16S rRNA databases can be crucial for various bioinformatics analyses, especially in microbiome research. However, it's important to note that databases can vary based on your specific needs, such as the taxonomic coverage you require or the type of analysis you're performing. Here's a general guideline on how you can obtain 16S rRNA databases:

NCBI (National Center for Biotechnology Information):
- NCBI provides various databases related to genetic information, including 16S rRNA sequences.
- You can access the 16S ribosomal RNA sequences from NCBI's Nucleotide database (https://www.ncbi.nlm.nih.gov/nucleotide/).
- Perform a search using keywords like "16S rRNA" or specific bacterial names to find relevant sequences.
- You can download sequences individually or in batches using the provided tools.
GreenGenes:
- GreenGenes is a widely used 16S rRNA gene sequence database.
- You can access it at http://greengenes.secondgenome.com/.
- GreenGenes provides precompiled databases for various purposes, including classification, alignment, and phylogenetic analysis.
SILVA:
- SILVA (https://www.arb-silva.de/) is another comprehensive database for ribosomal RNA (rRNA) sequences.
- It covers not only 16S rRNA but also other ribosomal RNA sequences.
- SILVA provides precompiled databases for various purposes, including taxonomic classification and alignment.
Ribosomal Database Project (RDP):
- RDP (http://rdp.cme.msu.edu/) is a curated database that offers 16S rRNA sequences.
- It provides tools for sequence analysis and classification.
- You can download sequences and taxonomy information from their website.
QIIME (Quantitative Insights Into Microbial Ecology):
- QIIME (https://qiime2.org/) is a widely used bioinformatics platform for microbiome analysis.
- It provides tools for analyzing microbial communities, including processing 16S rRNA sequences.
- QIIME often includes its own preprocessed 16S rRNA databases that can be used for analysis within the platform.

Before downloading any database, make sure to read the terms of use and citation requirements, as some databases may have specific usage policies. Additionally, consider the compatibility of the database with your analysis pipeline and software tools.

NCBI 16s RNA database location ftp://ftp.ncbi.nih.gov/blast/db/16SMicrobial.tar.gz

INC-Seq: accurate single molecule reads using nanopore sequencing

Jit — Mon, 27 Nov 2017 10:38:56 -0600

INC-Seq reads enabled accurate species-level classification, identification of species at 0.1 % abundance and robust quantification of relative abundances, providing a cheap and effective approach for pathogen detection and microbiome profiling on the MinION system.

Address of the bookmark: https://github.com/CSB5/INC-Seq

Heap: a highly sensitive and accurate SNP detection tool for low-coverage high-throughput sequencing data

Jit — Thu, 19 Apr 2018 08:06:03 -0500

Heap, that enables robustly sensitive and accurate calling of SNPs, particularly with a low coverage NGS data, which must be aligned to the reference genome sequences in advance. To reduce false positive SNPs, Heap determines genotypes and calls SNPs at each site except for sites at the both end of reads or containing a minor allele supported by only one read. Performance comparison with existing tools showed that Heap achieved the highest F-scores with low coverage (7X) restriction-site associated DNA sequencing reads of sorghum and rice individuals. This will facilitate cost-effective GWAS and GP studies in this NGS era. Code and documentation of Heap are freely available from https://github.com/meiji-bioinf/heap and our web site (http://bioinf.mind.meiji.ac.jp/lab/en/tools.html).

Address of the bookmark: https://github.com/meiji-bioinf/heap

P_RNA_scaffolder: a fast and accurate genome scaffolder using paired-end RNA-sequencing reads

Jit — Tue, 12 Jun 2018 08:14:41 -0500

P_RNA_scaffolder, a fast and accurate tool using paired-end RNA-sequencing reads to scaffold genomes. This tool aims to improve the completeness of both protein-coding and non-coding genes. After this tool was applied to scaffolding human contigs, the structures of both protein-coding genes and circular RNAs were almost completely recovered and equivalent to those in a complete genome, especially for long proteins and long circular RNAs.

Address of the bookmark: http://www.fishbrowser.org/software/P_RNA_scaffolder/

MSAProbs - Parallel and accurate multiple sequence alignment

Neel — Tue, 09 Jul 2019 23:58:44 -0500

MSAProbs is a well-established state-of-the-art multiple sequence alignment algorithm for protein sequences. The design of MSAProbs is based on a combination of pair hidden Markov models and partition functions to calculate posterior probabilities. Assessed using the popular benchmarks: BAliBASE, PREFAB, SABmark and OXBENCH, MSAProbs achieves statistically significant accuracy improvements over the existing top performing aligners, including ClustalW, MAFFT, MUSCLE, ProbCons and Probalign. In addition, MSAProbs is optimized for shared-memory CPUs by employing a multi-threaded design, and further parallelized for distributed-memory systems using MPI to overcome high memory overhead barrier and achieve good parallel and data-size scalability.

Address of the bookmark: http://msaprobs.sourceforge.net/homepage.htm#latest

CLARK: Fast, accurate and versatile sequence classification system

Jit — Sat, 15 Feb 2020 01:49:01 -0600

CLARK, a method based on a supervised sequence classification using discriminative k-mers. Considering two distinct specific classification problems (see the article for details), namely (1) the taxonomic classification of metagenomic reads to known bacterial genomes, and (2) the assignment of BAC clones and transcript to chromosome arms/centromeres (in the absence of a finished assembly for the reference genome), CLARK outperforms in classification speed and precision the best state-of-the-art methods.

http://clark.cs.ucr.edu/Spaced/

Address of the bookmark: http://clark.cs.ucr.edu/Spaced/

Liftoff: An accurate GFF3/GTF lift over pipeline

Neel — Sun, 20 Dec 2020 01:36:37 -0600

Liftoff is a tool that accurately maps annotations in GFF or GTF between assemblies of the same, or closely-related species. Unlike current coordinate lift-over tools which require a pre-generated “chain” file as input, Liftoff is a standalone tool that takes two genome assemblies and a reference annotation as input and outputs an annotation of the target genome.

Address of the bookmark: https://github.com/agshumate/Liftoff

HELIANO: A fast and accurate tool for detection of Helitron-like elements

LEGE — Tue, 13 Aug 2024 07:16:34 -0500

Helitron-like elements (HLE1 and HLE2) are DNA transposons. They have been found in diverse species and seem to play significant roles in the evolution of host genomes. Although known for over twenty years, Helitron sequences are still challenging to identify. Here, we propose HELIANO (Helitron-like elements annotator) as an efficient solution for detecting Helitron-like elements.

https://academic.oup.com/nar/advance-article/doi/10.1093/nar/gkae679/7730539?login=true

Address of the bookmark: https://github.com/Zhenlisme/heliano/