Get sequences for HMM hits from many inputs.
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genes-fasta concatenated-gene-alignment-fasta
contigs-db profile-db external-genomes internal-genomes hmm-source hmm-hits
This program can work with anvi’o contigs-db, external-genomes, or internal-genomes files to return sequences for HMM hits identified through the default anvi’o hmm-sources (such as the domain-specific single-copy core genes) or user-defined hmm-sources (such as HMMs for specific antibiotic resistance gene families or any other targets).
Using it with single-copy core genes in default anvi’o HMMs make it a very versatile tool for phylogenomics as the user can define specific sets of genes to be aligned and concatenated.
anvi-get-sequences-for-hmm-hits -c contigs-db \ --list-hmm-sources
AVAILABLE HMM SOURCES =============================================== * ‘Bacteria_71’ (type: singlecopy; num genes: 71) * ‘Archaea_76’ (type: singlecopy; num genes: 76) * ‘Protista_83’ (type: singlecopy; num genes: 83) * ‘Ribosomal_RNAs’ (type: Ribosomal_RNAs; num genes: 12)
anvi-get-sequences-for-hmm-hits -c contigs-db \ --hmm-source Bacteria_71 \ -o genes-fasta
Please note that the flag --list-available-gene-names
will give you the list of genes in an HMM collection (for example, for Bacteria_71
in the following use case), and it will not give you the list of genes in your genomes or metagenomes that are matching to them. You can generate a table of HMMs across your genomes or metagenomes with another program, anvi-script-gen-hmm-hits-matrix-across-genomes.
anvi-get-sequences-for-hmm-hits -c contigs-db \ --hmm-source Bacteria_71 \ --list-available-gene-names
* Bacteria_71 [type: singlecopy]: ADK, AICARFT_IMPCHas, ATP-synt, ATP-synt_A, Chorismate_synt, EF_TS, Exonuc_VII_L, GrpE, Ham1p_like, IPPT, OSCP, PGK, Pept_tRNA_hydro, RBFA, RNA_pol_L, RNA_pol_Rpb6, RRF, RecO_C, Ribonuclease_P, Ribosom_S12_S23, Ribosomal_L1, Ribosomal_L13, Ribosomal_L14, Ribosomal_L16, Ribosomal_L17, Ribosomal_L18p, Ribosomal_L19, Ribosomal_L2, Ribosomal_L20, Ribosomal_L21p, Ribosomal_L22, Ribosomal_L23, Ribosomal_L27, Ribosomal_L27A, Ribosomal_L28, Ribosomal_L29, Ribosomal_L3, Ribosomal_L32p, Ribosomal_L35p, Ribosomal_L4, Ribosomal_L5, Ribosomal_L6, Ribosomal_L9_C, Ribosomal_S10, Ribosomal_S11, Ribosomal_S13, Ribosomal_S15, Ribosomal_S16, Ribosomal_S17, Ribosomal_S19, Ribosomal_S2, Ribosomal_S20p, Ribosomal_S3_C, Ribosomal_S6, Ribosomal_S7, Ribosomal_S8, Ribosomal_S9, RsfS, RuvX, SecE, SecG, SecY, SmpB, TsaE, UPF0054, YajC, eIF-1a, ribosomal_L24, tRNA-synt_1d, tRNA_m1G_MT, Adenylsucc_synt
anvi-get-sequences-for-hmm-hits -c contigs-db \ --hmm-source Bacteria_71 \ --gene-names Ribosomal_L27,Ribosomal_L28,Ribosomal_L3 \ -o genes-fasta
anvi-get-sequences-for-hmm-hits -c contigs-db \ -p profile-db \ -C collection --hmm-source Bacteria_71 \ --gene-names Ribosomal_L27,Ribosomal_L28,Ribosomal_L3 \ -o genes-fasta
anvi-get-sequences-for-hmm-hits -c contigs-db \ -p profile-db \ -C collection --hmm-source Bacteria_71 \ --gene-names Ribosomal_L27,Ribosomal_L28,Ribosomal_L3 \ --get-aa-sequences \ -o genes-fasta
The resulting file can be used for phylogenomics analyses via anvi-gen-phylogenomic-tree or through more sophisticated tools for curating alignments and computing trees.
anvi-get-sequences-for-hmm-hits -c contigs-db \ -p profile-db \ -C collection --hmm-source Bacteria_71 \ --gene-names Ribosomal_L27,Ribosomal_L28,Ribosomal_L3 \ --get-aa-sequences \ --concatenate-genes \ --return-best-hit -o genes-fasta
You can play with this program using the anvi’o data pack for the infant gut data and by replacing the parameters above with appropriate ones in the following commands.
Download the latest version of the data from here:
doi:10.6084/m9.figshare.3502445
Unpack it:
tar -zxvf INFANTGUTTUTORIAL.tar.gz && cd INFANT-GUT-TUTORIAL
Import the collection merens
:
anvi-import-collection additional-files/collections/merens.txt \ -p PROFILE.db \ -c CONTIGS.db \ -C merens
Then run the program to
anvi-get-sequences-for-hmm-hits -p PROFILE.db \ -c CONTIGS.db \ -C merens \ -o OUTPUT.fa \ --hmm-source Campbell_et_al \ --gene-names Ribosomal_L27,Ribosomal_L28,Ribosomal_L3 \ --return-best-hit \ --get-aa-sequences \ --concatenate
Edit this file to update this information.
Are you aware of resources that may help users better understand the utility of this program? Please feel free to edit this file on GitHub. If you are not sure how to do that, find the __resources__
tag in this file to see an example.