Methods and systems for storing sequence read data
View Patent ↗The present invention generally relates to storing sequence read data. The invention can involve obtaining a plurality of sequence reads from a sample, identifying one or more sets of duplicative sequence reads within the plurality of sequence reads, and storing only one of the sequence reads from each set of duplicative sequence reads in a text file using nucleotide characters.
1. A method for storing sequence read data, the method comprising:
sequencing a nucleic acid from a sample to generate a plurality of sequence reads;
identifying one or more sets of duplicative sequence reads within the plurality of sequence reads;
storing only one sequence read from each of the one or more sets of duplicative sequence in a master read file;
collecting meta information for each of the plurality of sequence reads, appending the meta information into a compressed file, and matching the meta information to a single read in the master read file; and
later retrieving the plurality of sequence reads from the compressed file and the master read file.
2. A method for storing sequence read data, the method comprising:
obtaining a plurality of sequence reads from a sample by sequencing a nucleic acid from the sample;
identifying one or more sets of duplicative sequence reads within the plurality of sequence reads;
storing in a master read file only one sequence read from each of the one or more sets of duplicative sequence reads; and
separately retrieving the plurality of sequence reads from the master read file.
3. A method for using stored sequence read data, the method comprising:
using a computer system comprising a memory coupled to a processor for:
obtaining a master sequence read file that includes only one sequence read from each of one or more sets of duplicative sequence reads obtained from a sample and a compressed file that includes lines of metadata for the sequence reads obtained from the sample;
for each line of metadata in the compressed file, retrieving an associated read from the master sequence read file and appending that line of metadata and the associated read to an output sequence read file, wherein the output sequence read file contains the sequence reads as originally obtained from the sample.
4. The method of claim 3 , wherein the master sequence read file, the compressed file, and the output sequence read file each have a format that is human-readable.
5. The method of claim 4 , wherein sequence reads are stored in the master sequence read file and the output sequence read file using IUPAC characters.
6. The method of claim 4 , wherein the format of the output sequence read file is one selected from the group consisting of: a FASTA file; a FASTQ file; and a VCF file.
7. The method of claim 4 , wherein the format of the master sequence read file is a text file.
8. The method of claim 4 , wherein the computer system comprises a text editor program capable of opening the files having the format.
9. The method of claim 8 , wherein the text editor program is capable of displaying the files on a computer screen showing the metadata and the sequence reads in a human-readable format.
10. The method of claim 3 , wherein each line of metadata comprises a sequence read ID.
11. The method of claim 3 , wherein the output sequence read file contains a perfectly lossless retrieval of the sequence reads obtained from the sample.
12. The method of claim 3 , further comprising obtaining the master sequence read file and the compressed file by:
sequencing a nucleic acid from the sample to generate the sequence reads;
identifying the one or more sets of duplicative sequence reads within the sequence reads; and
storing the only one sequence read from each of the one or more sets of duplicative sequence reads in the master read file.