Sanrrone / extractSeq

Giving a contig name and positions (start and end), extractSeq can return the corresponding sequence from your fasta.

extractSeq

extracSeq is a bash script (awk embedded), that giving a contig name and positions (start and end), return the corresponding sequence from your fasta.

Usage

extractSeq need five (and intuitive), parameters (order is important):

• The contig name where are the coordinates that you want.
• Start position of your gene.
• End position of your gene.
• Fasta file to dive.
• Output name (optional, by default is "output").
• Strand where are your gene (default: +).

Example:

bash extractSeq.bash contig0001 500 2000 + myoutput Ecoli.fasta

This means that we dive in file Ecoli.fasta, searching the contig "contig0001" and then extract the sequence on the position 500 to 2000.

Real example: In the example folder there is a fasta (Ecoli.fasta), where the contigs names are like:

• NODE_1_length_350779_cov_17.5196
• NODE_2_length_328984_cov_17.2607

So, applying the usage will be:

bash extractSeq.bash NODE_1_length_350779_cov_17.5196 500 1400 - testgene example/Ecoli.fasta

This will give a testgene.fasta with the reverse complementary sequence.

Output

Following the same example, the output is a fasta (testgene.fasta), with the positions in the header indicating if are complement or not:

>NODE_1_length_350779_cov_17.5196 Ecoli.fasta c(500:1400)
TCTTTCGGTGTATTGTCCAGCTCCAGCGGCAGAGCCACGTTGCCAAAAACAGTACGCGAAG
AGAGCAGGTTAAAATGCTGGAAAATCATACCAATCTGGCGGCGAGCTTTGGTCAACTCGGA
TTCTGACAGCGTGGTCAGTTCCTGTCCATCGACCAGCACGCTACCCTCGGTTGGGCGCTCC
AGCAGGTTTACACAACGTATAAGCGTACTCTTACCCGCGCCTGAGGCACCGATAACGCCAT
AAATTTGCCCAGCTGGCACATGCAGGCTGACGTTGTTCAACGCCTGGATGGTGCGGGTGCC
CTGGTGGAACACTTTGGTGATATTCGAAAGTTTTATCATTGATTATTTATTATCGTCATTA
AGTTAGTCGTGGCATTTCGAATGCCTGAAACGGGCAACGCCGTCAATGAAATGGATGTTAA
GGCATCCAGACGTCTAAATCAATCAGGTTTATGCGAAGAGCACTTTCTTGCAGGTCGAAAC
ATGCGATACTAGCGTCACATGCCTTATTAAGGAGCTATAAAAGGTGGCGAAGAGCGTACCC
GCAATTTTTCTTGACCGTGATGGCACCATTAATGTCGATCACGGCTATGTCCATGAGATCG
ATAACTTTGAATTTATCGACGGTGTTATTGACGCCATGCGCGAGCTAAAAAAAATGGGCTT
CGCGCTGGTGGTAGTCACCAACCAGTCTGGCATTGCTCGCGGTAAATTTACTGAAGCACAG
TTTGAAACGCTGACCGAGTGGATGGACTGGTCGCTGGCGGACCGCGATGTCGATCTGGATG
GTATCTATTATTGCCCGCATCATCCGCAGGGTAGTGTTGAAGAGTTTCGCCAGGTCTGCGA
CTGCCGCAAACCACATCCGGGGATGCTTTTGT

WARNINGS

• Be careful with coordinates, if your contig have 100 nucleotides and you specify the coord 50,101. the script only write to 100.
• Make sure the coordinates begin from lower value to upper e.g (1 10, 400 425, etc).
• IUPAC ambiguity codes of the two possible nucleotides are converted as following: R↔Y, K↔M, S and W unchanged.
• Ambiguity codes of the three possible nucleotides are converted as following: B↔V, D↔H.
• Upper and lower case is preserved and can be used to mark regions of interest.

External useful tools

check for these tools to extract some useful information from your data:

• multiGenomicContext: Check the genomic context of several genomes or sequence just providing the GBK files.

• fetchMyLineage: Return the complete lineage of your organism just providing the genus and species names.

• extractSeq: Extract and size defined sequence from and specific contig, from and specific genome.

• plotMyGBK: Plot your GBK in a circular graph with COG categories.

• pasteTaxID: fetch the taxonomic IDs to your fastas.

• GGisy: Plot synteny of two sequence (you can use two genomes), and see the identity of the matched regions.

• getS2: obtain the order parameter to each residue of your simulation.