Methods for preparing nucleic acid libraries for sequencing
Processes and materials to detect cancer from a biopsy are described. In some cases, cell-free nucleic acids can be sequenced, and the sequencing result can be utilized to detect sequences derived from a neoplasm. Detection of somatic variants occurring in phase can indicate the presence of cancer in a diagnostic scan and a clinical intervention can be performed.
1. A method for preparing an enriched library of nucleic acids for sequencing, the method comprising:
identifying a patient-specific set of six or more genomic regions that harbor a plurality of phased variants that are within 170 base pairs of each other;
obtaining a personalized set of nucleic acid probes that have been designed to enrich for phased variant-containing nucleic acids from the six or more genomic regions;
preparing cell-free nucleic acids from the patient for sequencing; and
selectively enriching the prepared cell-free nucleic acids from the patient for phased variant-containing nucleic acids from the six or more genomic regions via hybridization capture or amplification to form an enriched library of nucleic acids for sequencing;
wherein identifying the patient-specific set of six or more genomic regions that harbor a plurality of phased variants comprises comparing sequencing data from a either a diseased sample from the patient or a cell-free DNA sample from the patient to sequencing data from a non-diseased sample from the patient;
wherein at least 10% of phased variant-containing nucleic acids from the library of nucleic acids have a first phased variant and a second phased variant that are separated from each other by at least one nucleotide.
2. The method of claim 1 , wherein the sequencing data from (1) the diseased sample or the cell-free DNA sample and (2) the sequencing data from the non-diseased sample are generated at least in part using whole genome sequencing or whole exome sequencing.
3. The method of claim 1 , wherein selectively enriching the prepared cell-free nucleic acids from the patient comprises enriching the cell-free nucleic acids for phased-variant containing molecules by at least 7,500-fold as compared to unenriched cell-free nucleic acids from the patient.
4. A method for preparing an enriched library of nucleic acids for sequencing, the method comprising:
identifying a patient-specific set of three or more genomic regions that harbor a plurality of phased variants that are within 170 base pairs of each other;
preparing cell-free nucleic acids from the patient for sequencing; and
selectively enriching the prepared cell-free nucleic acids from the patient for phased variant-containing nucleic acids from the three or more genomic regions to form an enriched library of nucleic acids for sequencing;
wherein at least 10% of phased variant-containing nucleic acids from the enriched library of nucleic acids have a first phased variant and a second phased variant that are separated from each other by at least one nucleotide.
5. The method of claim 4 , wherein identifying the patient-specific set of three or more genomic regions that harbor a plurality of phased variants comprises comparing sequencing data from a diseased sample from the patient to sequencing data from a non-diseased sample from the patient.
6. The method of claim 5 , wherein comparing sequencing data from the diseased sample from the patient to sequencing data from the non-diseased sample of the patient comprises aligning both the sequencing data from the diseased sample and the sequencing data from the non-diseased sample to a reference genome.
7. The method claim 5 , wherein the diseased sample is a cancerous sample.
8. The method of claim 7 , wherein the cancerous sample is a solid tumor.
9. The method of claim 7 , wherein the cancerous sample is not a lymphoma sample.
10. The method of claim 4 , wherein identifying the patient-specific set of three or more genomic regions that harbor a plurality of phased variants comprises comparing sequencing data from cell-free DNA of the patient to sequencing data from a non-diseased sample of the patient.
11. The method of claim 5 , wherein the sequencing data from the diseased sample and the sequencing data from the non-diseased sample are both generated at least in part using whole genome sequencing.
12. The method of claim 5 , wherein the sequencing data from the diseased sample and the sequencing data from the non-diseased sample are both generated at least in part using whole exome sequencing.
13. The method of claim 4 , wherein the set of three of more genomic regions comprises at least six different genomic regions.
14. The method of claim 4 , wherein the set of three or more genomic regions comprises at least seventeen different genomic regions.
15. The method of claim 4 , wherein the plurality of phased variants are somatic phased variants.
16. The method of claim 4 , further comprising:
designing a set of nucleic acid probes to enrich for phased variant-containing nucleic acids from the three or more genomic regions; and
obtaining the set of designed nucleic acid probes.
17. The method of claim 16 , wherein selectively enriching the prepared cell-free nucleic acids from the patient comprises using the set of designed nucleic acid probes to selectively capture cell-free nucleic acid molecules from three or more genomic regions that harbor the plurality of phased variants.
18. The method of claim 4 , wherein selectively enriching the prepared cell-free nucleic acids from the patient comprises enriching the cell-free nucleic acids for phased-variant containing molecules by at least 7,500-fold as compared to unenriched cell-free nucleic acids from the patient.
19. The method of claim 16 , wherein selectively enriching the prepared cell-free nucleic acids from the patient comprises selectively amplifying, using the designed nucleic acid probes, the cell-free nucleic acids from the patient for cell-free nucleic acids from the three or more genomic regions that harbor the plurality of phased variants.
20. The method of claim 4 , further comprising sequencing the enriched library of nucleic acids.
21. The method of claim 20 , wherein sequencing the enriched library of nucleic acids comprises sequencing to an average unique sequencing depth of at least 4000× across each genomic region of the set of three of more genomic regions.
22. The method of claim 20 , further comprising:
identifying a first set of molecules from the enriched library of nucleic acids that have doublet phased variants and a second set of molecules that have triplet phased variants; and
determining a phased-variant tumor fraction (PVAF) for each of the first set of molecules and the second set of molecules.
23. The method of claim 22 , further comprising:
identifying a third set of molecules from the enriched library of nucleic acids that have quadruplet phased variants; and
determining a phased-variant tumor fraction (PVAF) for each of the third set of molecules.
24. The method of claim 20 , wherein the enriched library of nucleic acids comprises at least 1,000 nucleic acid molecules.
25. The method of claim 20 , wherein the method does not comprise barcode-mediated error suppression of sequencing data from the enriched library of nucleic acids.
26. The method of claim 20 , further comprising performing barcode-mediated error suppression of sequencing data from the enriched library of nucleic acids.
27. The method of claim 4 , wherein the first phased variant and the second phased variant are both single nucleotide variants (SNVs).
28. The method of claim 4 , wherein the cell-free nucleic acids are selectively enriched from a plasma sample of the patient.
29. A method for detection or monitoring of a disease, the method comprising:
identifying a patient-specific set of three or more genomic regions that harbor a plurality of phased variants that are within 170 base pairs of each other;
preparing cell-free nucleic acids from the patient for sequencing;
selectively enriching the prepared cell-free nucleic acids from the patient for phased variant-containing nucleic acids from the three or more genomic regions to form an enriched library of nucleic acids for sequencing;
sequencing the enriched library of nucleic acids to produce sequencing data; and
analyzing the sequencing data to detect or monitor a disease of the patient;
wherein at least 10% of phased variant-containing nucleic acids from the library of nucleic acids have a first phased variant and a second phased variant that are separated from each other by at least one nucleotide.
30. The method of claim 29 , wherein the disease is a cancer.