How to extract the mobile genetic elements
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5.6 years ago
anabio86 • 0

Hi folks, I need to do alinhamento using just the chromosomal DNA, without the mobile genetic elements, I would like to know if there is a bioinformatic tools that can do it from fasta files? thx

Assembly alignment sequencing • 1.6k views
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I guess you could subset your reference FASTA file to include only the sequences you wish to include. What have you tried?

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Are you referring to masking parts of the genome that are repetitive before aligning? repeatmasker is the program used to do this. If you are working with human genome then repeat-masked versions are available.

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Actually, I am working with bacterial DNA, I need to perform a phylogenetic analysis using references from database, but before to compare with these references I need to remove the sequences that belonged to mobile genetic elements such as plasmids, phages this things

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mobile genetic elements

I think this can lead to some confusion. As a human geneticist I think of transposons when I read mobile genetic elements, and not phages/plasmids/....

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We need lots more information, such as what bacteria, whether it has completed reference genomes etc.

Detecting mobile elements is non-trivial. If your genome is not well curated already the task will be almost impossible. There is also not one single tool which will do all of this. Plasmid finding has its own set of tools (e.g. PlasFlow, PlasmidTron and others), prophages can be detected with PHAST/PHASTER (e.g.). I'm no expert on detection of transposons etc, but there are reviews out there which compare and benchmark many tools (e.g https://mobilednajournal.biomedcentral.com/articles/10.1186/s13100-015-0055-3 ).

You will largely have to try things and see what the results look like.

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I just gave up, seems impossible to do that

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Nothing is impossible. Why Portuguese ('alinhamento')?

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If I understand correctly, you are looking for FASTA files of chromosomes but not plasmids, right? If so, you can download them from NCBI using edirect as follows:

esearch -db assembly -q 'GCF_000008865.2' | elink -db assembly -target nuccore -name assembly_nuccore_refseq | efilter -q 'NOT plasmid[filter]' -source refseq | efetch -format fasta
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5.1 years ago

If you want to extract novel DNA mobile elements, then you need to findout the presence of Terminal Inverted Repeats and Target Site Duplications. You could predict the TIRs using EMBOSS Einverted Repeat Server and you can manually assess the presence of TSDs, in the case of DNA transposon/MITES (autonomous/non-autonomous). If you want to annotate your sequence based on the identified transposons, you can use censor repeat masking: https://www.girinst.org/censor/. Perhaps this is helpful: https://www.girinst.org/server/publ/AsDRF1/

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