Systems, methods, and compositions for viral-associated tumors
Contemplated systems and methods employ chimeric reference sequences that include a plurality of viral genome sequences to identify/quantify integration and co-amplification events. Most typically, the viral genome sequences are organized in the chimeric reference sequences as single chromosomes and the chimeric reference sequences are in BAM format.
1. A computer implemented method of identifying at least one of presence and integration of a nucleic acid of a pathogen in a nucleic acid sequence of a diseased mammalian tissue, comprising:
receiving, from a sequence database, a whole genome nucleic acid sequence from a reference mammalian tissue and at least one nucleic acid sequence of at least one pathogen;
merging the whole genome nucleic acid sequence from the reference mammalian tissue and the at least one nucleic acid sequence of the at least one pathogen to obtain a chimeric reference nucleic acid sequence;
identifying co-amplification of an oncogene sequence of the mammalian tissue and at least some of the nucleic acid sequence of the at least one pathogen;
formulating a solution, either circular or tandem duplication, for genomic rearrangement that includes the co-amplified sequences;
aligning, upon formulating the solution, the chimeric reference nucleic acid sequence and the oncogene of the diseased mammalian tissue using incremental synchronized alignment to identify at least one of presence and integration of the pathogen in the oncogene sequence of the nucleic acid sequence from the diseased mammalian tissue, and
wherein the pathogen is a virus selected from the group consisting of HTLV-1 (Human T-Cell Leukemia Virus), an HPV virus (Human Papillomavirus), HHV-8 (Human Herpes Virus 8), EBV (Epstein-Barr Virus), HBV (Hepatitis B Virus), HCV (Hepatitis C Virus), SV40 (Simian Vacuolating Virus 40), BKV (BK virus), JCV (JC virus), a HERV (human endogenous retrovirus), HMTV (human mammary tumor virus), KSHV (Kaposi's Sarcoma-Associated Herpesvirus), and TTV (Torque teno virus).
2. The method of claim 1 wherein the chimeric reference nucleic acid sequence comprises the at least one nucleic acid sequence of at least one pathogen and the mammalian nucleic acid sequence.
3. The method of claim 1 wherein the reference mammalian nucleic acid sequence is a matched normal mammalian nucleic acid sequence.
4. The method of claim 1 wherein the nucleic acid sequence from the mammalian tissue comprises at least nucleic acid sequences of one chromosome of the mammalian tissue.
5. The method of claim 1 wherein the nucleic acid sequence from the mammalian tissue comprises at least 50% of an exome of the mammalian tissue.
6. The method of claim 1 wherein the nucleic acid sequence from the mammalian tissue comprises at least 50% of an entire genome of the mammalian tissue.
7. The method of claim 1 wherein the chimeric reference nucleic acid sequence comprises nucleic acid sequences of a plurality of distinct pathogens.
8. The method of claim 1 further comprising a step of identifying an integration of at least some of the nucleic acid sequence of the at least one pathogen into the nucleic acid sequence from the mammalian tissue.