Genome annotation is a critical bottleneck in genomic research, especially for the comprehensive study of gene families in the genomes of non-model organisms. Despite the recent progress in automatic annotation, state-of-the-art tools used for this task often produce inaccurate annotations, such as fused, chimeric, partial or even completely absent gene models for many family copies, errors that require considerable extra efforts to be corrected. Here we present BITACORA, a bioinformatics tool that integrates popular sequence similarity-based search algorithms and Perl scripts to facilitate the curation of these inaccurate annotations and the identification of previously undetected gene family copies directly from genomic DNA sequences. The program creates general feature format (GFF) files, with both curated and newly identified gene models, and FASTA files with all predicted proteins. The output of BITACORA can be easily integrated in genomic annotation editors, greatly facilitating subsequent manual annotation and downstream analyses.
BITACORA documentation can be also be found in: http://www.ub.edu/softevol/bitacora/
BITACORA 1.3:
- BITACORA is able to use the latest GeMoMa version v1.7.1. However, v1.7.0 contains a bug that prevents our pipeline from working, please use v1.7.1 instead.
- Added a new script to call BITACORA with command line options (run first '$ chmod +x runBITACORA_command_line.sh' to make it executable, and '$ ./runBITACORA_command_line.sh -h' to see the available options)
BITACORA 1.2.1:
- Implementation of GeMoMa algorithm to reconstruct new gene models (set as default). The latest version tested in our pipeline is GeMoMa v1.6.4.
- New parameter that allows retaining novel proteins based on HMMER or BLASTP positive hits
- Additional step to conduct a more strict filtering of the output annotations in order to obtain a confident estimation on the number of gene members for a specific gene family.
- Installation
- Prerequisites
- Computational Requirements
- Usage modes
- 4.1 Full mode
- 4.2 Protein mode
- 4.3 Genome mode
- Parameters
- Running BITACORA
- Output
- Example
- Citation
- Troubleshooting
BITACORA is distributed as a multiplatform shell script (runBITACORA.sh) that calls several other Perl scripts, which include all functions responsible of performing all pipeline tasks. Hence, it does not require any installation or compilation step.
To run the pipeline edit the master script runBITACORA.sh variables described in Prerequisites, Data, and Parameters.
-
Perl: Perl is installed by default in most operating systems. See https://learn.perl.org/installing/ for installation instructions.
-
BLAST: Download blast executables from: ftp://ftp.ncbi.nlm.nih.gov/blast/executables/blast+/LATEST/
-
HMMER: The easiest way to install HMMER in your system is to type one of the following commands in your terminal:
% brew install hmmer # OS/X, HomeBrew
% port install hmmer # OS/X, MacPorts
% apt install hmmer # Linux (Ubuntu, Debian...)
% dnf install hmmer # Linux (Fedora)
% yum install hmmer # Linux (older Fedora)
% conda install -c bioconda hmmer # Anaconda
Or compile HMMER binaries from the source code: http://hmmer.org/
HMMER and BLAST binaries require to be added to the PATH environment variable. Specify the correct path to bin folders in the master script runBITACORA.sh, if necessary.
$ export PATH=$PATH:/path/to/blast/bin
$ export PATH=$PATH:/path/to/hmmer/bin
- GeMoMa: By default, BITACORA reconstructs new gene models using the GeMoMa algorithm (Keilwagen et al., 2016; 2018). The GeMoMa jar file (i.e. GeMoMa-1.6.4.jar) must be specified in GEMOMAP variable in runBITACORA.sh. GeMoMa is implemented in Java using Jstacs and can be downloaded from: http://www.jstacs.de/index.php/GeMoMa. The latest version of GeMoMa tested in our pipeline is v1.7.1.
GEMOMAP=/path/to/GeMoMa.jar (within runBITACORA.sh script)
BITACORA have been tested in UNIX-based platforms (both in Mac OS and Linux operating systems). Multiple threading can be set in blast searches, which is the most time-consuming step, by editing the option THREADS in runBITACORA.sh.
For a typical good quality genome (~2Gb in size and ~10,000 scaffolds) and a standard modern PC (16Gb RAM), a full run of BITACORA is completed in less than 24h. This running time, however, will depend on the size of the gene family or the group of genes surveyed in a particular analysis. For gene families of 10 to 100 members, BITACORA spends from minutes to a couple of hours.
In case of larger or very fragmented genomes, BITACORA should be used in a computer cluster or workstation given the increase of RAM memory and time required.
BITACORA has been initially designed to work with genome sequences and protein annotations (full mode). However, the pipeline can also be used either with only protein or only genomic sequences (protein and genome modes, respectively). These last modes are explained in next subsections.
Preparing the data: The input files (in plain text) required by BITACORA to run a full analysis are (update the complete path to these files in the master script runBITACORA.sh):
[NOTE: mRNA or transcript, and CDS are mandatory fields]
GFF3 example
lg1_ord1_scaf1770 AUGUSTUS gene 13591 13902 0.57 + . ID=g1;
lg1_ord1_scaf1770 AUGUSTUS mRNA 13591 13902 0.57 + . ID=g1.t1;Parent=g1;
lg1_ord1_scaf1770 AUGUSTUS start_codon 13591 13593 . + 0 Parent=g1.t1;
lg1_ord1_scaf1770 AUGUSTUS CDS 13591 13902 0.57 + 0 ID=g1.t1.CDS1;Parent=g1.t1
lg1_ord1_scaf1770 AUGUSTUS exon 13591 13902 . + . ID=g1.t1.exon1;Parent=g1.t1;
lg1_ord1_scaf1770 AUGUSTUS stop_codon 13900 13902 . + 0 Parent=g1.t1;
BITACORA also accepts other GFF formats, such as Ensembl GFF3 or GTF.
[NOTE: GFF formatted files from NCBI can cause errors when processing the data, use the supplied script “reformat_ncbi_gff.pl” (located in the folder /Scripts/Tools) to make the file parsable by BITACORA]. See Troubleshooting in case of getting errors while parsing your GFF.
Ensembl FF3 example
AFFK01002511 EnsemblGenomes gene 761 1018 . - . ID=gene:SMAR013822;assembly_name=Smar1;biotype=protein_coding;logic_name=ensemblgenomes;version=1
AFFK01002511 EnsemblGenomes transcript 761 1018 . - . ID=transcript:SMAR013822-RA;Parent=gene:SMAR013822;assembly_name=Smar1;biotype=protein_coding;logic_name=ensemblgenomes;version=1
AFFK01002511 EnsemblGenomes CDS 761 811 . - 0 Parent=transcript:SMAR013822-RA;assembly_name=Smar1
AFFK01002511 EnsemblGenomes exon 761 811 . - . Parent=transcript:SMAR013822-RA;Name=SMAR013822-RA-E2;assembly_name=Smar1;constitutive=1;ensembl_end_phase=0;ensembl_phase=0;rank=2;version=1
BITACORA requires identical IDs for proteins and their corresponding mRNAs or transcripts IDs in the GFF3.
[NOTE: we recommend using genes but not isoforms in BITACORA; We provide the following script Scripts/Tools/exclude_isoforms_fromfasta.pl to cluster isoforms, keeping the longest sequence as representative. Isoforms could also be removed or properly annotated after BITACORA analysis]
IV. Specific folder with files containing the query protein databases (YOURFPDB_db.fasta) and HMM profiles (YOURFPDB_db.hmm) in FASTA and hmm format, respectively, where the “YOURFPDB” label is your specific data file name. The addition of ”_db” to the database name with its proper extension, fasta or hmm, is mandatory.
BITACORA requires one protein database and profile per surveyed gene family (or gene group). See Example/DB files for an example of searching for two different gene families in BITACORA: OR, Odorant Receptors; and CD36-SNMP.
[NOTE: profiles covering only partially the proteins of interest are not recommended]
HMM profiles are found in InterPro or PFAM databases associated to known protein domains. If you don't know if your protein contains any described domain, you can search in InterPro (http://www.ebi.ac.uk/interpro/) using the protein sequence of one of your queries to identify domains. For example, for the chemosensory proteins (CSPs) in insects, you can download the HMM profile from pfam (Curation & model PFAM submenu): http://pfam.xfam.org/family/PF03392#tabview=tab6
In the case of searching for proteins with not described protein domains, or with domains not covering most of the protein sequence, it should be performed an alignment of the query proteins to create a specific HMM profile. Example of building a protein profile (it requires an aligner, here we use mafft as example):
$ mafft --auto FPDB_db.fasta > FPDB_db.aln
$ hmmbuild FPDB_db.hmm FPDB_db.aln
[NOTE: BITACORA could be used without an HMM profile, although it is not recommended. To do so, create the YOURFPDB_db.hmm file containing any random line, and set the parameter 'GENOMICBLASTP=T', or '-b T' if using the command line script (and ignore any warning related to HMM)]
The proteins included in the database (FPDB) and that will be used as query in similarity-based searches are really important. The inclusion of proteins or protein fragments unrelated with the focal gene family will lead to false positive identifications.
On the other hand, if possible, we recommend including proteins from phylogenetically close species to increase the power of similarity-based searches, particularly in fast-evolving and old gene families. If the organism of interest does not have an annotated genome of a close related species, we recommend to perform a second BITACORA round (step 3 described in the manuscript; Figure 1), by including in the query database (sFPDB) all sequences identified in the first round along with a new HMM profile built with these updated protein set.
BITACORA can also run with a set of proteins (i.e. predicted proteins from transcriptomic data; script runBITACORA_protein_mode.sh) by using the input files described in points III and IV of the section 4.1.
Under this mode, BITACORA identifies, curates when necessary, and report all members of the surveyed family among the predicted proteins. The original protein sequences (not being curated) are also reported (located in Intermediate_Files if cleaning output is active).
BITACORA can also run with raw genome sequences (i.e., not annotated genomes; script runBITACORA_genome_mode.sh), by using the input files described in points I and IV of the section 4.1.
Under this mode, BITACORA identifies de novo all members of the surveyed family and returns a BED file with gene coordinates of the detected exons, a FASTA file with predicted proteins from these exons and a GFF3 file with the corresponding structural annotations.
[NOTE: By default, BITACORA applies GeMoMa software to generate accurate gene models, but it requires the additional installation of some dependencies. Otherwise, BITACORA can use the “close-proximity” algorithm to generate gene models, although these models are only semi-automatic predictions that could require further manual annotation (e.g. using genomic annotation editor). Under this genome mode, we highly recommend running a second iterative search round.]
- The option CLEAN can be used to create the Intermediate_files directory where all intermediate files will be stored (see output section).
CLEAN=T #T=true, F=false
- BLAST and HMMER hits are filtered with a default cut-off E-value of 10e-5 (in addition to an internal parameter for filtering the length covered by the alignment). E-value can be modified in the master script runBITACORA.sh.
EVALUE=10e-5 #Default
- Number of threads to be used in blast searches, default is 1.
THREADS=1 #Default
- BITACORA can generate new gene models (for those putative genes not included in the input GFF) using two different methods. By default (GEMOMA=T), BITACORA will use the GeMoMa software to predict novel genes from TBLASTN alignments (the user must specify the PATH to jar file in GEMOMAP variable described in prerequisites). Otherwise (GEMOMA=F), BITACORA will predict new genes by exon proximity (close-proximity method described in the manuscript).
GEMOMA=T #Default
- For the close proximity method (GEMOMA=F option), BITACORA uses by default an upper limit value of 15 kb to join putative exons from separate but contiguous (and in the same scaffold) genome hits to build a gene model This value can be modified in the master script runBITACORA.sh.
MAXINTRON=15000 #Default
- New generated gene models are subsequently evaluated for the presence of the specific protein family domain using either HMMER or BLASTP searches against the proteins in FPDB (GENOMICBLASTP=T option). Otherwise (GENOMICBLASTP=F), BITACORA will only retain all gene models exhibiting the protein domain using HMMER. Despite that the first option is more sensitive, poor quality annotations in the FPDB could lead to a loss of specificity.
GENOMICBLASTP=F #Default
- An additional validation and filtering step of the resulting annotations can be conducted using the option ADDFILTER. If ADDFILTER=T, BITACORA will cluster highly similar sequences (with 98% identity; which could represent isoforms or resulting from putative assembly artifacts), and will discard all annotations with a length lower than the specified in FILTERLENGTH parameter. This step can also be run independently using the script Scripts/Tools/ exclude_similar_sequences_infasta_andgff.pl. It allows obtaining a good estimation of the copy number for a particular gene family, without the overestimation of this value by including isoforms or putative assembly artifacts.
ADDFILTER=T #Default
FILTERLENGTH=30 #Default
We highly recommend the use of GeMoMa (set as default) to construct more accurate gene models. This method incorporates intron position conservation as evidence in gene predictions. Nevertheless, in the presence of sequencing or assembly errors and pseudogenes (e.g. highly fragmented assemblies or point mutations either real or introduced by the sequencing process), this algorithm might fail to identify some genes; in these cases, the close proximity method is able to report these gene models regardless of whether they are true or artifactual pseudogenes or fragmented copies. Therefore, we encourage the user to apply both methods in order to ensure the identification of all gene family copies, functional or not.
MAXINTRON is a key parameter affecting the quality of gene models built using the close-proximity algorithm in BITACORA step 2. BITACORA is distributed with a script (get_intron_size_fromgff.pl) that computes the mean, median, and 95% and 99% upper limits of intron length in a specific genome (from the GFF of the genome) or for a specific gene family (from the GFF generated in BITACORA output).
As default, BITACORA uses a (conservative) high intron length for the algorithm, in order to ensure joining all exons of a same gene. However, a large value of MAXINTRON parameter can generate gene fusions. These possible gene fusions are tagged with the label “Ndom” in the corresponding proteins in the output file, being N the number of predicted domains (i.e., likely different genes).
The number of predicted gene fusions identified de novo (i.e, in not annotated DNA regions) can be obtained using the following command in the terminal:
$ grep '>.*dom' DB/DB_genomic_and_annotated_proteins_trimmed.fasta
After preparing the data as indicated in steps 5 (Usage) and 6 (Parameters), you can execute BITACORA with the following command:
$ bash runBITACORA.sh
BITACORA creates an output folder for each query database, and three files with the number of proteins identified in each step, including a summary table. For the genome and protein modes, only one summary table will be reported with the number of identified genes.
In each folder, there are the following main files (considering you chose to clean output directory. If not, all files will be found in the same output folder):
- YOURFPDB_genomic_and_annotated_genes_trimmed.gff3: GFF3 file with information of all curated models.
- YOURFPDB_genomic_and_annotated_proteins_trimmed.fasta: A fasta file containing the protein sequences corresponding to the curated models.
Non-redundant data: Relevant information excluding identical proteins or those considered as false positives (e.g. duplicated scaffolds, isoforms…).
- YOURFPDB_genomic_and_annotated_genes_trimmed_nr.gff3: GFF3 file containing all non-redundant curated models.
- YOURFPDB_genomic_and_annotated_proteins_trimmed.fasta: A fasta file containing the non-redundant protein sequences corresponding to the curated models.
Note: Applying the parameter ADDFILTER=T, BITACORA will report additional files with more stringent filtering and clustering.
- YOURFPDB_genomic_and_annotated_genes_trimmed_idseqsclustered.gff3
- YOURFPDB_genomic_and_annotated_genes_trimmed_idseqsclustered.fasta
BED files with the location of TBLASTN hits in the genome sequence:
- YOURFPDBtblastn_parsed_list_genomic_positions_nogff_filtered.bed: BED file with the genomic coordinates of all TBLASTN hits.
- YOURFPDBtblastn_parsed_list_genomic_positions.bed: BED file with the genomic coordinates of the TBLASTN hits involving putative novel exons (i.e. absent in the input GFF).
In addition, BITACORA generates the following Intermediate files (located into Intermediate_files folder if CLEAN=T). These files contain information of some intermediate steps of the analysis, such as the original or untrimmed gene models, and multiples files stored for debugging or as controls:
- YOURFPDB_annot_genes.gff3 and YOURFPDB_proteins.fasta: GFF3 and FASTA files containing the original untrimmed models and proteins of all genes identified in the Step 1 (Fig. 1). (Fig. 1 BITACORA workflow).
- YOURFPDB_annot_genes_trimmed.gff3 and YOURFPDB_proteins_trimmed.fasta: GFF3 and FASTA files containing the curated models for the proteins identified and annotated in the Step 1 (Fig. 1).
- YOURFPDB_genomic_genes.gff3: GFF3 file containing the untrimmed structural annotations for the proteins identified in BITACORA Step 2 (Fig. 1).
- YOURFPDB_genomic_genes_trimmed.gff3: GGFF3 file containing the structural annotations for the proteins identified in BITACORA Step 2 (Fig. 1) after curation based in HMM profile or BLASTP hits.
- /Hmmer folder containing the output of HMMER searches against both previously annotated and newly identified proteins.
- /GeMoMa folder containing the raw gene models obtained with GeMoMa.
- YOURFPDBgfftrimmed.cds.fasta and YOURFPDBgfftrimmed.pepfasta: Files containing the CDS and protein sequences from YOURFPDB_annot_genes_trimmed.gff3 (used for debugging purposes)
- YOURFPDBgffgenomictrimmed.cds.fasta and YOURFPDBgffgenomictrimmed.pep.fasta: Files containing CDS and protein sequences translated directly from YOURFPDB_genomic_genes_trimmed.gff3
- YOURFPDB_blastp.outfmt6: BLASTP output of the searches that use FPDB as a query against the annotated proteins.
- YOURFPDB_tblastn.outfmt6: : TBLASTN output of the searches that use FPDB as a query against the genomic sequence.
- YOURFPDB_blastp_parsed_list.txt; YOURFPDB_hmmer_parsed_list.txt; YOURFPDB_allsearches_list.txt; YOURFPDB_combinedsearches_list.txt: Parsed coordinate files combining all hits from BLASTP and HMMER outputs.
- YOURFPDB_tblastn_parsed_list_genomic_positions.txt and YOURFPDB_tblastn_parsed_list_genomic_positions_notgff_filtered.txt Files containing coordinates of parsed TBLASTN results.
- YOURFPDB_prots_VsGFF_badannot_list.txt and YOURFPDB_goodannot_list.txt: Debugging files: Debugging files: Files to check the perfect match between the identified proteins and the GFF3 annotations. If the file badannot_list.txt is not empty, the GFF3 has annotation errors (from the original GFF3). Please, search in "YOURFPDB_genomic_and_annotated_proteins_trimmed_nr.fasta" for the correct protein in any of the two other reading frames. Once you find the correct translation, modify the GFF3 by adding 1 or 2 nucleotide position in the start of the GFF3 (check the strand). If you are unable to fix this problem, please report the error via GitHub.
- YOURFPDB_genomic_genes_proteins.fasta: FASTA file containing the raw predicted protein sequences encoded in novel gene models obtained in BITACORA Step 2 (Fig. 1). Note that this file has not been subjected to the HMMER or BLASTP filter and some annotations could contain errors.
- YOURFPDB_genomic_exon_proteins.fasta: FASTA file with the exon sequences that have been joined into genes in the aforementioned file (in case of using the close-proximity method).
- Additional generated files are stored for pipeline debugging and controls.
The proteins identified with BITACORA can be used either for further prospective analyses or to facilitate a more curated annotation using genome annotation editors (such as Apollo). In the first case, it is recommended to perform some validation of the newly identified proteins, especially when using the close proximity algorithm. It is important to determine if gene models need to be split or joined (i.e., if the parameter MAXINTRON needs to be modified). For highly divergent gene families, we also recommend using the parameter BLASTPHMMER=T in order to identify distant homologs. In addition, we provide some scripts in Tools to cluster highly similar sequences or discard small protein fragments in order to obtain a curated set of annotations for a gene family (i.e. clustering isoforms and putative genome assembly artifacts as duplicated scaffolds that would provide an erroneous estimation of the number of genes). Moreover, it would be also useful to build an MSA, constructing a tree of the gene family including members of other closely related species, or checking for characteristic structural features of the protein (i.e. the presence of transmembrane domains, signal peptides, etc.). See Vizueta et al. (2018) for some examples. Finally, the output annotations can be classified as complete or partial genes based on the average length of the gene family domain using the script provided in Tools (get_genes_partial_pseudo.pl).
In the second case, BITACORA is also designed to facilitate the annotation of the generated gene models in editors as Apollo. The specific files that can be used for this purpose are (see an example in Documentation/example_Apollo.png):
- Original GFF3
- Final GFF3 with curated models for the annotated proteins
- BED files from TBLASTN search
An example to run BITACORA can be found in Example folder. First, unzip the Example_files.zip file to obtain the necessary files for BITACORA. In this example, two chemosensory-related gene families in insects: Odorant receptors (ORs), and the CD36-SNMP gene family; will be searched in the chromosome 2R of Drosophila melanogaster. The GFF3 and protein files are modified from original annotations, deleting some gene models, to allow that BITACORA can identify novel not-annotated genes.
To run the example, edit the master script runBITACORA.sh to add the path to BLAST and HMMER binaries and run the script. It will take around 1 minute with 2 threads.
$ bash runBITACORA.sh
Joel Vizueta, Alejandro Sánchez-Gracia, Julio Rozas. BITACORA: A comprehensive tool for the identification and annotation of gene families in genome assemblies. Molecular Ecology Resources, 2020. https://doi.org/10.1111/1755-0998.13202
Joel Vizueta, Julio Rozas, Alejandro Sánchez-Gracia; Comparative Genomics Reveals Thousands of Novel Chemosensory Genes and Massive Changes in Chemoreceptor Repertories across Chelicerates, Genome Biology and Evolution, Volume 10, Issue 5, 1 May 2018, Pages 1221–1236, https://doi.org/10.1093/gbe/evy081
Moreover, if you use GeMoMa, please cite:
J. Keilwagen, M. Wenk, J. L. Erickson, M. H. Schattat, J. Grau, and F. Hartung. Using intron position conservation for homology-based gene prediction. Nucleic Acids Research, 2016. https://doi.org/10.1093/nar/gkw092
J. Keilwagen, F. Hartung, M. Paulini, S. O. Twardziok, and J. Grau Combining RNA-seq data and homology-based gene prediction for plants, animals and fungi. BMC Bioinformatics, 2018. https://doi.org/10.1186/s12859-018-2203-5
When BITACORA detects any error related to input data, it stops and prints the description of the error. Please check the error and your data.
If you are getting errors related to parsing the GFF file, consider that BITACORA expects proteins ID to be as ID in mRNA rows from GFF3. In case of protein ID and mRNA ID causing error as they are not named equally, first, you can use the script located in Scripts/Tools/get_proteins_notfound_ingff.pl to check which proteins are not found in the GFF3 file, as detailed in the Error message. You could use only those proteins found in the GFF3 in BITACORA. If all proteins are named differently in the GFF3, you can obtain a protein file from the GFF3 using the script Scripts/gff2fasta_v3.pl and use that protein file as input to BITACORA. You could also modify the perl module Readgff.pm to allow BITACORA to read your data. Otherwise, modify the GFF, preferably, as GFF3 format.
If you cannot solve the error, create an issue in Github specifying the error and all details as possible.
React
Typescript
Django
Laravel
Facebook
Microsoft
Google
Alibaba
D3
Tencent