
What is the difference between FASTA, FASTQ, and SAM file …
FASTA file format is a DNA sequence format for specifying or representing DNA sequences and was first described by Pearson (Pearson,W.R. and Lipman,D.J. (1988) Improved tools for biological sequence comparison. Proc. Natl Acad. Sci. USA, 85, 2444–2448)
How to download FASTA sequences from NCBI using the terminal?
Nov 7, 2019 · esearch -db nucleotide -query "NC_030850.1" | efetch -format fasta > NC_030850.1.fasta. And you should find your fasta sequence downloaded. As you have several sequences to download, I think it will be quite easy to add this command into a little bash script to process all of them.
phylogenetics - Understanding the fasta file format and using edit ...
Jul 28, 2020 · Your understanding of FASTA format is about right. The type of basic problem you're eluding to we term "sequence alignment"- edit distance might be okay for teaching but in practise we use other algorithms, e.g. you might be interested in the Needleman–Wunsch or Smith–Waterman algorithms.
samtools - How to create a .bed file from .fasta? - Bioinformatics ...
I have some problems in creating a .bed file for hg19, so I will be able to visualize the .bed file in IGV. The .fasta file contains rows of this form: >chr1:0-1000
trnascan se - convert tRNA coordinates Result to Fasta format ...
Oct 11, 2018 · You can select “Output BED format” on the tRNAscan-SE server: Given the output BED format and your input reference in FASTA format, you can easily generate a FASTA file of tRNA sequences via bedtools getfasta: bedtools getfasta -name -s -fo ‹output.fasta› -fi ‹reference.fasta› -bed ‹tRNAscan-SE-output.bed›
How to convert fasta alignment to nexus or phylip format?
Aug 29, 2022 · The advantage here is you can select what phylip format you want. That is a BIG advantage, traditional phylip format is terrible, particularly with taxa ids lengths. Here relaxed phylip format is being used. The other advantages, Easily parse, change, alter the taxa names; Phylip taxa id can be ANY length (id_width=); save it as a script;
How to identify the DNA sequence of a gene in the complete …
Jun 9, 2021 · My method was the following: I downloaded the FASTA format file of the complete genome sequence of the archaea organism that I am studying, that is CP003685, and then I downloaded the CDS file from NCBI by clicking on ">Send to>Coding Sequencing>FASTA Nucleotide>Create File". In this way I have a txt file (always FASTA format file) in which I ...
How to convert FASTA to BED - Bioinformatics Stack Exchange
May 19, 2017 · Otherwise, any Bio* library (Perl, Python, Ruby) provides FASTA format parsers which will extract sequence IDs and lengths. I'd point out that whilst this resembles BED it is not, strictly-speaking, since BED maps to coordinates on a …
Help to create a dataframe in Python from a FASTA file
Jan 15, 2022 · I want to create a dataframe in Python starting from a FASTA format file. Given the toy FASTA file that I am attaching, I built this program in Python that returns four colums corresponding to id, sequence length, sequence, animal …
Convert FASTA to FASTQ with dummy quality scores
Jan 20, 2020 · fastaq to_fake_qual in.fasta - | fastaq fasta_to_fastq in.fasta - out.fastq The first tool, to_fake_qual, creates fake quality scores (default 40) for each base and the -sends that file (.qual) to stdout. The second tool, fasta_to_fastq, consumes both the original fasta and the quality scores coming from stdin and turns these into a fastq file.