Sponsored Content
Top Forums UNIX for Beginners Questions & Answers How to count the length of fasta sequences? Post 303033663 by dineshkumarsrk on Wednesday 10th of April 2019 05:43:26 AM
Old 04-10-2019
is it possible to print the order as same as id.txt. The command works fine, but the order has been changed. For example, id.txt file listed the headers as follows,
Code:
seq1
seq2

Where as my unique.fasta file has the sequences in the following order,
Code:
>seq2
ATGCTTA
>seq1
GCTAGT

But, the command print seq2 length first followed by seq1 as shown below.
Code:
seq2     7
seq1      6

Therefore, is it possible to keep the order as same as id.txt.

--- Post updated at 09:43 AM ---

Dear singh,
Is it possible to print the order as same as id.txt. The command works fine, but the order has been changed. For example, id.txt file listed the headers as follows,
Code:
seq1
seq2

Whereas, my unique.fasta file has the sequences in the following order,
Code:
>seq2
ATGCTTA
>seq1
GCTAGT

But, the command print seq2 length first followed by seq1 as shown below.
Code:
seq2     7
seq1    6

Therefore, is it possible to keep the order as same as id.txt.
 

10 More Discussions You Might Find Interesting

1. Shell Programming and Scripting

Extract length wise sequences from fastq file

I have a fastq file from small RNA sequencing with sequence lengths between 15 - 30. I wanted to filter sequence lengths between 21-25 and write to another fastq file. how can i do that? (4 Replies)
Discussion started by: empyrean
4 Replies

2. Shell Programming and Scripting

Shell script for changing the accession number of DNA sequences in a FASTA file

Hi, I am having a file of dna sequences in fasta format which look like this: >admin_1_45 atatagcaga >admin_1_46 atatagcagaatatatat with many such thousands of sequences in a single file. I want to the replace the accession Id "admin_1_45" similarly in following sequences to... (5 Replies)
Discussion started by: margarita
5 Replies

3. Shell Programming and Scripting

Extract sequences from a FASTA file based on another file

I have two files. File1 is shown below. >153L:B|PDBID|CHAIN|SEQUENCE RTDCYGNVNRIDTTGASCKTAKPEGLSYCGVSASKKIAERDLQAMDRYKTIIKKVGEKLCVEPAVIAGIISRESHAGKVL KNGWGDRGNGFGLMQVDKRSHKPQGTWNGEVHITQGTTILINFIKTIQKKFPSWTKDQQLKGGISAYNAGAGNVRSYARM DIGTTHDDYANDVVARAQYYKQHGY >16VP:A|PDBID|CHAIN|SEQUENCE... (7 Replies)
Discussion started by: nelsonfrans
7 Replies

4. Shell Programming and Scripting

Count and search by sequence in multiple fasta file

Hello, I have 10 fasta files with sequenced reads information with read sizes from 15 - 35 . I have combined the reads and collapsed in to unique reads and filtered for sizes 18 - 26 bp long unique reads. Now i wanted to count each unique read appearance in all the fasta files and make a table... (5 Replies)
Discussion started by: empyrean
5 Replies

5. Shell Programming and Scripting

Shorten header of protein sequences in fasta file

I have a fasta file as follows >sp|O15090|FABP4_HUMAN Fatty acid-binding protein, adipocyte OS=Homo sapiens GN=FABP4 PE=1 SV=3 MCDAFVGTWKLVSSENFDDYMKEVGVGFATRKVAGMAKPNMIISVNGDVITIKSESTFKN TEISFILGQEFDEVTADDRKVKSTITLDGGVLVHVQKWDGKSTTIKRKREDDKLVVECVM KGVTSTRVYERA >sp|L18484|AP2A2_RAT AP-2... (3 Replies)
Discussion started by: alexypaul
3 Replies

6. UNIX for Dummies Questions & Answers

Select distinct sequences from fasta file and list

Hi How can I extract sequences from a fasta file with respect a certain criteria? The beginning of my file (containing in total more than 1000 sequences) looks like this: >H8V34IS02I59VP SDACNDLTIALLQIAREVRVCNPTFSFRWHPQVKDEVMRECFDCIRQGLG YPSMRNDPILIANCMNWHGHPLEEARQWVHQACMSPCPSTKHGFQPFRMA... (6 Replies)
Discussion started by: Marion MPI
6 Replies

7. Shell Programming and Scripting

Getting unique sequences from multiple fasta file

Hi, I have a fasta file with multiple sequences. How can i get only unique sequences from the file. For example my_file.fasta >seq1 TCTCAAAGAAAGCTGTGCTGCATACTGTACAAAACTTTGTCTGGAGAGATGGAGAATCTCATTGACTTTACAGGTGTGGACGGTCTTCAGAGATGGCTCAAGCTAACATTCCCTGACACACCTATAGGGAAAGAGCTAAC >seq2... (3 Replies)
Discussion started by: Ibk
3 Replies

8. Shell Programming and Scripting

Outputting sequences based on length with sed

I have this file: >ID1 AA >ID2 TTTTTT >ID-3 AAAAAAAAA >ID4 TTTTTTGGAGATCAGTAGCAGATGACAG-GGGGG-TGCACCCC Add I am trying to use this script to output sequences longer than 15 characters: sed -r '/^>/N;{/^.{,15}$/d}' The desire output would be this: >ID4... (8 Replies)
Discussion started by: Xterra
8 Replies

9. Shell Programming and Scripting

Shorten header of protein sequences in fasta file to only organism name

I have a fasta file as follows >sp|Q8WWQ8|STAB2_HUMAN Stabilin-2 OS=Homo sapiens OX=9606 GN=STAB2 PE=1 SV=3 MMLQHLVIFCLGLVVQNFCSPAETTGQARRCDRKSLLTIRTECRSCALNLGVKCPDGYTM ITSGSVGVRDCRYTFEVRTYSLSLPGCRHICRKDYLQPRCCPGRWGPDCIECPGGAGSPC NGRGSCAEGMEGNGTCSCQEGFGGTACETCADDNLFGPSCSSVCNCVHGVCNSGLDGDGT... (3 Replies)
Discussion started by: jerrild
3 Replies

10. UNIX for Beginners Questions & Answers

How to add specific bases at the beginning and ending of all the fasta sequences?

Hi, I have to add 7 bases of specific nucleotide at the beginning and ending of all the fasta sequences of a file. For example, I have a multi fasta file namely test.fasta as given below test.fasta >TalAA18_Xoo_CIAT_NZ_CP033194.1:_2936369-2939570:+1... (1 Reply)
Discussion started by: dineshkumarsrk
1 Replies
ABACAS(1)							   User Commands							 ABACAS(1)

NAME
abacas - Algorithm Based Automatic Contiguation of Assembled Sequences SYNOPSIS
abacas -r ref -q qs -p prog [OPTIONS] OR abacas -r ref -q psf -e ref reference sequence in a single fasta file qs contigs in multi-fasta format rog MUMmer program to use: 'nucmer' or 'promer' psf pseudomolecule/ordered sequence file in fasta format OPTIONS -h print usage -d use default nucmer/promer parameters -s int minimum length of exact matching word (nucmer default = 12, promer default = 4) -m print ordered contigs to file in multifasta format -b print contigs in bin to file -N print a pseudomolecule without "N"s -i int mimimum percent identity [default 40] -v int mimimum contig coverage [default 40] -V int minimum contig coverage difference [default 1] -l int minimum contig length [default 1] -t run tblastx on contigs that are not mapped -g string (file name) print uncovered regions (gaps) on reference to file name -a append contigs in bin to the pseudomolecule -o prefix output files will have this prefix -P pick primer sets to close gaps -f int number of flanking bases on either side of a gap for primer design (default 350) -R int Run mummer [default 1, use -R 0 to avoid running mummer] -e Escape contig ordering i.e. go to primer design -c Reference sequence is circular DESCRIPTION
ABACAS is intended to rapidly contiguate (align, order, orientate), visualize and design primers to close gaps on shotgun assembled contigs based on a reference sequence. ABACAS uses MUMmer to find alignment positions and identify syntenies of assembled contigs against the reference. The output is then pro- cessed to generate a pseudomolecule taking overlapping contigs and gaps in to account. ABACAS generates a comparision file that can be used to visualize ordered and oriented contigs in ACT. Synteny is represented by red bars where colour intensity decreases with lower values of percent identity between comparable blocks. Information on contigs such as the orientation, percent identity, coverage and overlap with other contigs can also be visualized by loading the outputted feature file on ACT. AUTHOR
ABACAS IS Copyright (C) 2008-10 The Wellcome Trust Sanger Institute, Cambridge, UK. This manual page was written by Andreas Tille <tille@debian.org>, for the Debian project (and may be used by others). 1.3.1 2011-02-11 ABACAS(1)
All times are GMT -4. The time now is 11:52 PM.
Unix & Linux Forums Content Copyright 1993-2022. All Rights Reserved.
Privacy Policy