B-cell Repertoire Inductive Lineage and Immunosequence Annotator
BRILIA is designed to be a single-platform software capable of processing B-cell receptor sequences, annotating VDJ junctions, assigning B-cell lineages/clonotypes, and characerizing B-cell repertoires.
CONTACT
E-mail: brilia@bhsai.org (address to Donald Lee for BRILIA help, or Sid Chuadhury for all other questions)
Hours: M-F, 9am-5pm EST, off on federal holidays
- Accepts DNA/RNA sequence files with the following extensions:
- .fasta or .fa
- .fastq (see MinQuality input parameter to treat low-quality base reads as "N" bases)
- .csv (comma-delimited)
- .ssv (semicolon-delimited)
- .tsv (tab-delimited)
- Does not accept unassembled, paired-end reads. These should be assembled using another software.
- Non-ACGTU letters are treated as wildcard "N" bases. Special letters are not used yet (Ex: R for A/G will be treated as N)
- For delimited files, make sure that the first row is the data header. Ex: "SeqName, H-Seq, L-Seq, TemplateCount"
- SeqName: the name of the sequence
- H-Seq: heavy chain sequence
- L-Seq: light chain sequence
- TemplateCount: the number of sequence copies (Optional)
- See example input files
- Returns 3 delimited csv file:
- [output_file_name].BRILIAv3.csv : final annotation and phylogeny data of productive V(D)J sequences
- [output_file_name].BRILIAv3.Raw.csv : initial annotation of V(D)J sequences without lineage-base annotation correction.
- [output_file_name].BRILIAv3.Err.csv : non-productive VDJ sequences and any sequences that could not be annotated fully.
- If the output file is not specified, files will be stored in a subfolder with the same name as the input file.
- See output file header info
- See example output files
- Dowload & install the MATLAB Runtime R2017a(9.2) from MathWorks into a folder, referred to as
RUNTIME_FOLDER
. - Download & unzip the BRILIA exe files into a folder, referred to as
BRILIA_FOLDER
. - Open the OS terminal and navigate to
BRILIA_FOLDER
. - Run BRILIA. If the OS asks for permission to modify files, "cancel" should work. See here for more details.
Windows> BRILIA.exe
Linux$ run_BRILIA.sh RUNTIME_FOLDER
You should end up with a prompt like this:
BRILIA>
Assuming the files are structured as such:
/home/user/my files/file1.fastq
file2.fastq
fileN.fastq
Output files will be placed as such:
/home/user/my files/file1/file1.BRILIAvN.csv
file2/file2.BRILIAvN.csv
fileN/fileN.BRILIAvN.csv
BRILIA> ? (see help)
BRILIA> cd "/home/user/my files" (go to sequece file parent folder. Use quotes "" if there is a space in the path)
BRILIA> "./file*.fastq" -chain h -species mouse -strain balb (process heavy chain for mouse balb/c)
Developed at BHSAI (bhsai.org)
Website: https://github.com/bhsai/brilia
Status: ...
Status: Finished in 3.3 sec.
BRILIA> mergeSimilarSeq "./*" 0.01 (optional: parent-child sequences with < 1% Hamming distance will be merged under the parent)
BRILIA> runAnalysis "./*" (run analysis on all output files in subfolder of this current folder)
Status: Drawing 46 trees.
Status: ...
BRILIA> exit
- Consider adding
BRILIA_FOLDER
( andRUNTIME_FOLDER
for Linux ) to the OSPATH
to call BRILIA easily. - You could skip entering the
BRILIA>
prompt by adding inputs after the command in step 4. Example:
Windows> BRILIA.exe species mouse chain h ...
Linux$ run_BRILIA.sh RUNTIME_FOLDER species mouse chain h ...
- To test if BRILIA is working, try the following:
BRILIA> test all
A folder calledExamples
will be generated in theBRILIA_FOLDER
and BRILIA will process these folders. - For Linux, make sure executable files have read (r) + execute (x) permissions. Add permissions if needed.
BRILIA_FOLDER$ chmod +rx BRILIA BRILIA_FOLDER$ chmod +rx run_BRILIA.sh
- The program is distributed under the GNU General Public License.
- BRILIA patch info.
- Feature requests and open issues.