Methods of enriching for and identifying polymorphisms
View Patent ↗The invention encompasses methods for enriching for and identifying a polymorphism within a nucleic acid sample either by separating a subset of a nucleic acid sample or by selectively replicating a subset of a nucleic acid sample such that the polymorphism is contained within a nucleic acid population with reduced complexity, and then identifying the polymorphism within the enriched nucleic acid sample. Methods also are disclosed for enriching for and identifying a polymorphism by contacting a nucleic acid sample that includes a subset of nucleic acid molecules having a sequence that binds to a sequence-specific binding activity with a molecule having a sequence-specific binding activity under conditions which permit specific binding, such that the subset of nucleic acid molecules bound to the activity is enriched for nucleic acid molecules having the sequence recognized by the sequence-specific binding activity, and detecting a polymorphism with respect to a reference sequence in the subset of nucleic acid molecules.
1. A process that can be used to identify in a nucleic acid sample the presence or absence of nucleic acid sequence differences, wherein each said difference is with respect to one or more reference sequences, the process comprising:
a. fragmenting nucleic acids in said sample;
b. linking adapter sequences to the nucleic acid fragments generated in step a;
c. binding said nucleic acid fragments to a solid support to form bound nucleic acid fragments, and amplifying said bound nucleic, acid fragments; and
d. identifying nucleic acid sequences within said amplified nucleic acid fragments.
2. The process of claim 1 wherein there are a plurality of solid supports which each immobilizes separation elements which bind said nucleic acid fragments to the solid supports.
3. The process of claim 2 wherein the separation elements effect separation by interacting with or hybridizing to the adapter sequences.
4. The process of claim 2 wherein the solid supports are beads or a nylon or nitrocellulose membrane having an oligonucleotide capable of hybridizing to the adapter sequences attached to the nucleic acid fragments.
5. The process of claim 4 wherein the beads are agarose or cellulose or paramagnetic beads.
6. The process of claim 1 wherein sequence differences are identified in at least 10,000 nucleic acid fragments.
7. The process of claim 1 wherein the fragmenting is with restriction enzyme digestion.
8. The process of claims 1 wherein the nucleic acid fragments are amplified before or after step b of claim 1 .
9. The process of claim 1 wherein the identifying of nucleic acid sequences in step (d) includes hybridizing sequencing primers to the amplified nucleic acid fragments.
10. The process of claim 9 wherein the sequencing primers are extended following hybridization.
11. The process of claim 1 wherein the adapter sequences are operatively linked to the nucleic acid fragments in step (b).
12. The process of claim 1 wherein the adapter sequences are ligated to the nucleic acid fragments in step (b).
13. The process of claim 1 wherein the identifying of nucleic acid sequences in step (d) includes hybridizing, sequencing primers to the bound and amplified fragments and ligating the sequencing primers to oligonucleotides which are also hybridized to the bound and amplified fragments.