CODEWITHSUNDEEP
linuxbioinformaticsfasta
Tezie
Tezie

Reputation: 67

How to retrieve sequences from a Fasta file by gene ID

I know this question has been asked a hundred times but I've been at it all day and I can't seem to make this work. I have a fasta file that looks like this ...

>BGI_novel_T016697 Solyc03g033550.3.1
CTGACGTATACAATTAAGCCGCGAAAAATCTACTTTTTTTTTAATAGATATGAATTTCTTTTGTTTCGTATAATGAAGTATTTGTTCCAACAATGTTTAATTATTAGGCATTTGGAATGTGATGGGGCAACTAACAAAGAAGCCAATATCAACATCAATTAACAAACATATGATATAATTCTAGTGAAGTGAAAGCCAAGATATGAAACTCTCCACCCACACTATCTTAAATGATCTTTTTTAAAACATTCTAATTAGGTGATAACTAAAAGCAATAATTCTACCAATTTTGAAACAAACAATATGGTCCC
>BGI_novel_T016313 Solyc03g025570.2.1
TTCAAGTGTTAGTTTCACATCATCACGTTTGGACCTACGTTTCTATATTAGAACATATTCTAACTGATCTCTAGCTGTTATTCATGGGATTGTAAGAAATTTGTATCCCTCTCCGGATTTTACTTTGATCGCCACAAAATGAACATATGCTTTCAATTTTCTATGATGAAAAATCAGCCTCTCTCAATATTGGGTTTAAA
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAGAGGAGATTTTCCCAACAGTTTTCATTTACACACATGGGTTAAGTATTCATAAATAAAAGAGAAAAATCTGTTTATAAGTTGGAGAGTAGTATAAATACAGGAGATTTTCCCAACAGTTTTCATTTATACACATGGGTTAAGTATTCTTAAATAGAAAATCGGAAGTATTATAAATTCTCACTCAAAGAAACCACGTTTGCTCATTTTCGTTATTCCCTTAAAAACATGGGAAGATGAAAGAAAAAAACTAACACATAAAAAGATTGTGAGTTTACTTATTCATGGAGAATTCCCCATTTAAGTTGACAATATTTTTCTATGGTCTTGAACGGCCAGAAAAGTTAATATCCACAACTATTTTCCACTCAATAAGTGTTCCGATACCGTTGAACTTTTTAATATTTTGCACGCCCTTCGTGAAATGTTTTACTCCGTTACTGTCGCGATAATGATGTTTAAAAT
>BGI_novel_T016817 BGI_novel_G001220
GCCCAAGTCATAGGTAGTGCCTGTGCGGGTTGACACTCAACATGTGACCGCCACCACATTTTGGCATTTCCCTGAAACTGATAGGTTACAAACTCAATGCCAAATCATTCCACTATGCCCATTTTATGTAGTAACTCATGACAATCAACCAGAAAATCGTAGGCATCCTCAGATTCAGCACCCTTGAAGACTGGAGGTTTCAATTTCAAGAACTTACTGAAAAATTCATGCTGATCACTTGTCATTATAGGCCCTGTAGTCAAACGAGGAAACGTGCCTATTTCCAATGAGGCATCCATG
>BGI_novel_T016141 Solyc03g007600.3.1

and I want to retrieve the sequences that match the gene IDs from a .txt file:

Solyc00g256710.2.1
Solyc01g010890.3.1
Solyc01g056990.3.1
Solyc01g060050.2.1
Solyc01g081120.2.1
Solyc01g097740.3.1
Solyc01g098180.3.1
Solyc01g102320.1.1
Solyc01g106420.3.1
Solyc01g111580.3.1
Solyc01g111970.3.1
Solyc02g005530.2.1
Solyc02g031780.1.1
Solyc02g064595.1.1
Solyc02g081920.3.1
Solyc02g084220.3.1

Now, I have already tried samtools and FaSomeRecords, but both these methods produce no output. I guess it's because the title also contains transcript IDs (which I can ignore) Do you guys have any suggestions for me? please let me know if you require additional information. Cheers!

Upvotes: 3

Views: 5829

Answers (4)

drmrgd
drmrgd

Reputation: 733

Since a FASTA construct is a two line pair consisting of a defline (e.g. >BGI_novel_T016697 Solyc03g033550.3.1) followed by a line that contains the sequence, you can probably use the --after-context argument to grep to return the matched line followed by the next line. None of the gene IDs in your example are in the example FASTA file you gave, but if I add a matching gene ID to that file for testing, you can see how it works.

Gene lookup file:

$ cat lookup.txt
cat lookup.txt
Solyc00g256710.2.1
Solyc01g010890.3.1
Solyc01g056990.3.1
Solyc01g060050.2.1
Solyc01g081120.2.1
Solyc01g097740.3.1
Solyc01g098180.3.1
Solyc01g102320.1.1
Solyc01g106420.3.1
Solyc01g111580.3.1
Solyc01g111970.3.1
Solyc02g005530.2.1
Solyc02g031780.1.1
Solyc02g064595.1.1
Solyc02g081920.3.1
Solyc02g084220.3.1
Solyc03g080075.1.1

Sequence FASTA file:

$ cat seqs.fa
>BGI_novel_T016697 Solyc03g033550.3.1
CTGACGTATACAATTAAGCCGCGAAAAATCTACTTTTTTTTTAATAGATATGAATTTCTTTTGTTTCGTATAATGAAGTATTTGTTCCAACAATGTTTAATTATTAGGCATTTGGAATGTGATGGGGCAACTAACAAAGAAGCCAATATCAACATCAATTAACAAACATATGATATAATTCTAGTGAAGTGAAAGCCAAGATATGAAACTCTCCACCCACACTATCTTAAATGATCTTTTTTAAAACATTCTAATTAGGTGATAACTAAAAGCAATAATTCTACCAATTTTGAAACAAACAATATGGTCCC
>BGI_novel_T016313 Solyc03g025570.2.1
TTCAAGTGTTAGTTTCACATCATCACGTTTGGACCTACGTTTCTATATTAGAACATATTCTAACTGATCTCTAGCTGTTATTCATGGGATTGTAAGAAATTTGTATCCCTCTCCGGATTTTACTTTGATCGCCACAAAATGAACATATGCTTTCAATTTTCTATGATGAAAAATCAGCCTCTCTCAATATTGGGTTTAAA
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAGAGGAGATTTTCCCAACAGTTTTCATTTACACACATGGGTTAAGTATTCATAAATAAAAGAGAAAAATCTGTTTATAAGTTGGAGAGTAGTATAAATACAGGAGATTTTCCCAACAGTTTTCATTTATACACATGGGTTAAGTATTCTTAAATAGAAAATCGGAAGTATTATAAATTCTCACTCAAAGAAACCACGTTTGCTCATTTTCGTTATTCCCTTAAAAACATGGGAAGATGAAAGAAAAAAACTAACACATAAAAAGATTGTGAGTTTACTTATTCATGGAGAATTCCCCATTTAAGTTGACAATATTTTTCTATGGTCTTGAACGGCCAGAAAAGTTAATATCCACAACTATTTTCCACTCAATAAGTGTTCCGATACCGTTGAACTTTTTAATATTTTGCACGCCCTTCGTGAAATGTTTTACTCCGTTACTGTCGCGATAATGATGTTTAAAAT
>BGI_novel_T016817 BGI_novel_G001220
GCCCAAGTCATAGGTAGTGCCTGTGCGGGTTGACACTCAACATGTGACCGCCACCACATTTTGGCATTTCCCTGAAACTGATAGGTTACAAACTCAATGCCAAATCATTCCACTATGCCCATTTTATGTAGTAACTCATGACAATCAACCAGAAAATCGTAGGCATCCTCAGATTCAGCACCCTTGAAGACTGGAGGTTTCAATTTCAAGAACTTACTGAAAAATTCATGCTGATCACTTGTCATTATAGGCCCTGTAGTCAAACGAGGAAACGTGCCTATTTCCAATGAGGCATCCATG

Grep command with -w for whole word matching (in case you might get a partial result), -f to use a file of terms / patters to search, and -A1 to return the next line after a match:

$ grep -w -f lookup.txt -A1 seqs.fa
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAGAGGAGATTTTCCCAACAGTTTTCATTTACACACATGGGTTAAGTATTCATAAATAAAAGAGAAAAATCTGTTTATAAGTTGGAGAGTAGTATAAATACAGGAGATTTTCCCAACAGTTTTCATTTATACACATGGGTTAAGTATTCTTAAATAGAAAATCGGAAGTATTATAAATTCTCACTCAAAGAAACCACGTTTGCTCATTTTCGTTATTCCCTTAAAAACATGGGAAGATGAAAGAAAAAAACTAACACATAAAAAGATTGTGAGTTTACTTATTCATGGAGAATTCCCCATTTAAGTTGACAATATTTTTCTATGGTCTTGAACGGCCAGAAAAGTTAATATCCACAACTATTTTCCACTCAATAAGTGTTCCGATACCGTTGAACTTTTTAATATTTTGCACGCCCTTCGTGAAATGTTTTACTCCGTTACTGTCGCGATAATGATGTTTAAAAT

Unless you have some complex pattern matching and / or some post processing that needs to be done, I think a simple grep should get you there a little more simply.

Upvotes: 1

tink
tink

Reputation: 15204

And a small awk alternative:

With the fasta file looking like this:

$ cat fasta 
>BGI_novel_T016697 Solyc03g033550.3.1
CTGACGTATACAATTAAGCCGCGAAAAATCTACTTTTTTTTTAATAGATATGAATTTCTTTTGTTTCGTATAATGAAGTATTTGTTCCAACAATGTTTAATTATTAGGCATTTGGAATGTGATGGGGCAACTAACAAAGAAGCCAATATCAACATCAATTAACAAACATATGATATAATTCTAGTGAAGTGAAAGCCAAGATATGAAACTCTCCACCCACACTATCTTAAATGATCTTTTTTAAAACATTCTAATTAGGTGATAACTAAAAGCAATAATTCTACCAATTTTGAAACAAACAATATGGTCCC
>BGI_novel_T016313 Solyc03g025570.2.1
TTCAAGTGTTAGTTTCACATCATCACGTTTGGACCTACGTTTCTATATTAGAACATATTCTAACTGATCTCTAGCTGTTATTCATGGGATTGTAAGAAATTTGTATCCCTCTCCGGATTTTACTTTGATCGCCACAAAATGAACATATGCTTTCAATTTTCTATGATGAAAAATCAGCCTCTCTCAATATTGGGTTTAAA
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAGAGGAGATTTTCCCAACAGTTTTCATTTACACACATGGGTTAAGTATTCATAAATAAAAGAGAAAAATCTGTTTATAAGTTGGAGAGTAGTATAAATACAGGAGATTTTCCCAACAGTTTTCATTTATACACATGGGTTAAGTATTCTTAAATAGAAAATCGGAAGTATTATAAATTCTCACTCAAAGAAACCACGTTTGCTCATTTTCGTTATTCCCTTAAAAACATGGGAAGATGAAAGAAAAAAACTAACACATAAAAAGATTGTGAGTTTACTTATTCATGGAGAATTCCCCATTTAAGTTGACAATATTTTTCTATGGTCTTGAACGGCCAGAAAAGTTAATATCCACAACTATTTTCCACTCAATAAGTGTTCCGATACCGTTGAACTTTTTAATATTTTGCACGCCCTTCGTGAAATGTTTTACTCCGTTACTGTCGCGATAATGATGTTTAAAAT
>BGI_novel_T016817 BGI_novel_G001220
GCCCAAGTCATAGGTAGTGCCTGTGCGGGTTGACACTCAACATGTGACCGCCACCACATTTTGGCATTTCCCTGAAACTGATAGGTTACAAACTCAATGCCAAATCATTCCACTATGCCCATTTTATGTAGTAACTCATGACAATCAACCAGAAAATCGTAGGCATCCTCAGATTCAGCACCCTTGAAGACTGGAGGTTTCAATTTCAAGAACTTACTGAAAAATTCATGCTGATCACTTGTCATTATAGGCCCTGTAGTCAAACGAGGAAACGTGCCTATTTCCAATGAGGCATCCATG
>BGI_novel_T016141 Solyc03g007600.3.1
GCCCAAGTCATAGGTAGTGCCTGTGCGGGTTGACACTCAACATGTGACCGCCACCACATTTTGGCATTTCCCTGAAACTGATAGGTTACAAACTCAATGCCAAATCATTCCACTATGCCCATTTTATGTAGTAACTCATGACAATCAACCAGAAAATCGTAGGCATCCTCAGATTCAGCACCCTTGAAGACTGGAGGTTTCAATTTCAAGAACTTACTGAAAAATTCATGCTGATCACTTGTCATTATAGGCCCTGTAGTCAAACGAGGAAACGTGCCTATTTCCAATGAGGCATCCATG

The ID file a.txt like that:

$ cat a.txt 
Solyc00g256710.2.1
Solyc01g010890.3.1
Solyc01g056990.3.1
Solyc01g060050.2.1
Solyc01g081120.2.1
Solyc01g097740.3.1
Solyc01g098180.3.1
Solyc01g102320.1.1
Solyc01g106420.3.1
Solyc01g111580.3.1
Solyc01g111970.3.1
Solyc02g005530.2.1
Solyc02g031780.1.1
Solyc02g064595.1.1
Solyc02g081920.3.1
Solyc02g084220.3.1
Solyc03g080075.1.1
Solyc03g007600.3.1

We can do this:

$ awk 'FNR==NR{a[$0]++} FNR!=NR{if($NF in a){print $0; getline; print}}' a.txt fasta 
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAGAGGAGATTTTCCCAACAGTTTTCATTTACACACATGGGTTAAGTATTCATAAATAAAAGAGAAAAATCTGTTTATAAGTTGGAGAGTAGTATAAATACAGGAGATTTTCCCAACAGTTTTCATTTATACACATGGGTTAAGTATTCTTAAATAGAAAATCGGAAGTATTATAAATTCTCACTCAAAGAAACCACGTTTGCTCATTTTCGTTATTCCCTTAAAAACATGGGAAGATGAAAGAAAAAAACTAACACATAAAAAGATTGTGAGTTTACTTATTCATGGAGAATTCCCCATTTAAGTTGACAATATTTTTCTATGGTCTTGAACGGCCAGAAAAGTTAATATCCACAACTATTTTCCACTCAATAAGTGTTCCGATACCGTTGAACTTTTTAATATTTTGCACGCCCTTCGTGAAATGTTTTACTCCGTTACTGTCGCGATAATGATGTTTAAAAT
>BGI_novel_T016141 Solyc03g007600.3.1
GCCCAAGTCATAGGTAGTGCCTGTGCGGGTTGACACTCAACATGTGACCGCCACCACATTTTGGCATTTCCCTGAAACTGATAGGTTACAAACTCAATGCCAAATCATTCCACTATGCCCATTTTATGTAGTAACTCATGACAATCAACCAGAAAATCGTAGGCATCCTCAGATTCAGCACCCTTGAAGACTGGAGGTTTCAATTTCAAGAACTTACTGAAAAATTCATGCTGATCACTTGTCATTATAGGCCCTGTAGTCAAACGAGGAAACGTGCCTATTTCCAATGAGGCATCCAT

Explanation of the awk-stanza: FNR==NR{a[$0]++}

While we operate on the first file, the IDs, we add each ID to an array;

FNR!=NR{if($NF in a){print $0; getline; print}}'

When we reach the fast file we take the last field $NF of each line and check it it exists in the array; if it does we print the line and the line following it.

Upvotes: 1

tomc
tomc

Reputation: 1207

It has been a while for me but the defline
(the first line in a fasta record that begins with >) needs to be in particular format to be indexed for sequence retrieval.

many years (decades) ago I would construct deflines like

>gi|123|lcl|xyz ...

so sequences could be retrieved with 'xyz' where 'lcl' was a builtin blast "local" namespace to go along with the default indexed ones.

here you go:

https://en.wikipedia.org/wiki/FASTA_format

coerce your defines to a supported index-able format
re-index then enjoy your very rapid sequence retrieval.

this won't help much if your sequence database is small and not worth the indexing effort.

In those cases I would just used a fasta_grep perl script I had found online somewhere ...

it might have been this one.

http://web.mit.edu/meme_v4.11.4/share/doc/fasta-grep.html

Upvotes: 1

Timur Shtatland
Timur Shtatland

Reputation: 12347

Use a Perl one-liner, grep and seqtk subseq to extract the desired fasta sequences:

# Create test input:

cat > in.fasta <<EOF
>BGI_novel_T016697 Solyc03g033550.3.1
CTGACGTATACAATTAAGCCGCG
>BGI_novel_T016313 Solyc03g025570.2.1
TTCAAGTGTTAGTTTCACATCAT
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAG
>BGI_novel_T016817 BGI_novel_G001220
GCCCAAGTCATAGGTAGTGCCTG
>BGI_novel_T016141 Solyc03g007600.3.1
ACGTACGTACGTACGTACGTACG
EOF

cat > gene_ids.txt <<EOF
Solyc03g033550.3.1
Solyc03g080075.1.1
Solyc00g256710.2.1
Solyc01g010890.3.1
EOF

# Extract ids and gene ids into a tsv file:
perl -lne '@f = /^>(\S+)\s+(\S+)/ and print join "\t", @f;' in.fasta > ids_gene_ids.tsv

# Select ids that correspond to the desired gene ids:
grep -f gene_ids.txt ids_gene_ids.tsv | cut -f1 > ids.selected.txt

# Extract fasta sequence that correspond to desired gene ids:
seqtk subseq in.fasta ids.selected.txt > out.fasta                

cat out.fasta

Output:

>BGI_novel_T016697 Solyc03g033550.3.1
CTGACGTATACAATTAAGCCGCG
>BGI_novel_T018109 Solyc03g080075.1.1
GCAAGGGAAAGAAGTATTACTAG

Note that seqtk can be installed, for example, using conda.

Upvotes: 1

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