Methods for simultaneous amplification of target loci
The invention provides methods for simultaneously amplifying multiple nucleic acid regions of interest in one reaction volume as well as methods for selecting a library of primers for use in such amplification methods. The invention also provides library of primers with desirable characteristics, such as minimal formation of amplified primer dimers or other non-target amplicons.
1. A method for amplifying and sequencing DNA, comprising:
tagging isolated cell free DNA with one or more universal tail adaptors to generate tagged products, wherein the isolated cell-free DNA is isolated from a blood sample collected from a subject who is not a pregnant women;
amplifying the tagged products one or more times to generate final amplification products, wherein one of the amplification steps comprises targeted amplification of a plurality of single nucleotide polymorphism (SNP) loci in a single reaction volume, wherein one of the amplifying steps introduces a barcode and one or more sequencing tags; and
sequencing the plurality of SNP loci on the cell free DNA by conducting massively parallel sequencing on the final amplification products, wherein the plurality of SNP loci comprises 25-2,000 loci associated with cancer.
2. The method of claim 1 , wherein tagging the cell free DNA comprises ligating the one or more universal tail adaptors to the cell free DNA.
3. The method of claim 2 , wherein the one or more universal tail adaptors each comprise a first strand and a second strand, wherein a first end of each of the universal tail adaptors comprises a double-stranded section comprising the 5′ portion of the first strand and the 3′ portion of the second strand, wherein the first end is ligated to the cell free DNA.
4. The method of claim 3 , wherein amplifying the tagged products comprises a first amplifying step and a second amplifying step, wherein the first amplifying step comprises using a first target-specific primer that specifically anneals to a target sequence and a first adaptor primer having a nucleotide sequence identical to a first portion of the first strand to generate a first amplification product.
5. The method of claim 4 , wherein the second amplifying step comprises using a second target-specific primer that specifically anneals to the first amplification product and a second adaptor primer having a nucleotide sequence identical to a second portion of the first strand to generate the final amplification product.
6. The method of claim 5 , wherein the second adaptor primer is nested relative to the first adaptor primer.
7. The method of claim 6 , wherein the second target-specific primer comprises an index tag.
8. The method of claim 7 , wherein the second amplifying step further comprises using an index primer comprising a sequence complementary to the index tag.
9. The method of claim 8 , wherein the index primer comprises the barcode and a first sequencing tag.
10. The method of claim 1 , wherein the one or more universal tail adaptors comprise a second barcode.
11. The method of claim 1 , wherein the one or more universal tail adaptors comprise a second sequencing tag.
12. The method of claim 1 , wherein the one or more universal tail adaptors comprise a first universal tail adaptor and a second universal tail adaptor.
13. The method of claim 12 , wherein tagging the cell free DNA comprises amplifying the cell free DNA with a first primer comprising the first universal tail adaptor and a second primer comprising the second universal tail adaptor.
14. The method of claim 12 , wherein amplifying the tagged products comprises a single amplifying step.
15. The method of claim 14 , wherein amplifying the tagged products comprises using a third primer and a fourth primer, wherein the third primer comprises a first sequencing tag and wherein the fourth primer comprises a second sequencing tag.