HIGH SENSITIVITY MUTATION DETECTION USING SEQUENCE TAGS
The invention is directed to methods for increasing the sensitivity of high throughput sequencing, particularly for distinguishing true rare mutations from amplification, sequencing and other sample processing errors that occur in sequencing techniques. In one aspect, methods of the invention includes steps of (a) preparing templates from nucleic acids in a sample; (b) labeling by sampling the templates to form tag-template conjugates, wherein substantially every template of a tag-template conjugate has a unique sequence tag; (c) linearly amplifying the tag-template conjugates; (d) generating a plurality of sequence reads from the linearly amplified tag-template conjugates; and (e) determining a nucleotide sequence of each of the nucleic acids based on the frequencies, or numbers, of each type of nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
1 . A method for sequencing nucleic acids comprising:
preparing templates from nucleic acids in a sample;
labeling by sampling the templates to form tag-template conjugates, wherein substantially every template of a tag-template conjugate has a unique sequence tag;
linearly amplifying the tag-template conjugates;
generating a plurality of sequence reads from the linearly amplified tag-template conjugates; and
determining a nucleotide sequence of each of the nucleic acids based on the frequencies of each type of nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
2 . A method for determining a nucleotide sequence of a rare nucleic acid, the method comprising the steps of:
attaching sequence tags to nucleic acids from a sample to form tag-template conjugates, wherein substantially every nucleic acid of the tag-template conjugates has a unique sequence tag;
linearly amplifying the tag-template conjugates;
generating a plurality of sequence reads from the linearly amplified tag-template conjugates; and
determining a nucleotide sequence of each of the nucleic acids based on the frequencies of each type of nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
3 . A method for determining a nucleotide sequence of a rare nucleic acid, the method comprising the steps of:
attaching sequence tags to nucleic acids from a sample to form tag-template conjugates, wherein substantially every nucleic acid of the tag-template conjugates has a unique sequence tag;
linearly amplifying the tag-template conjugates so that an amplicon is formed comprising only copies or copies of copies of the tag-template;
generating a plurality of sequence reads for each copy of the tag-template conjugates in the amplicon; and
determining a nucleotide sequence of each of the nucleic acids based on the frequencies of each type of nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
4 . The method of claim 1 wherein said template or said nucleic acid is single stranded DNA.
5 . The method of claim 1 wherein said step of generating a plurality of sequence reads comprises separately amplifying each of said tag-template conjugates and sequencing each of the separately amplified tag-template conjugates to provide said sequence reads.
6 . The method of claim 5 wherein said step of separately amplifying is carried out h bridge PCR or emulsion PCR.
7 . The method of claim 1 wherein said step of determining includes determining a plurality nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
8 . The method of claim 7 wherein said plurality nucleotide at each of said nucleotide positions is a majority of nucleotides at such position.
9 . The method of claim 1 wherein said step of linearly amplifying is carried out by asymmetric PCR, NASBA or RCA.
10 . The method of claim 2 wherein said template or said nucleic acid is single stranded DNA.
11 . The method of claim 2 wherein said step of generating a plurality of sequence roads comprises separately amplifying each of said tag-template conjugates and sequencing each of the separately amplified tag-template conjugates to provide said sequence reads.
12 . The method of claim 11 wherein said step of separately amplifying is carried out by bridge PCR or emulsion PCR.
13 . The method of claim 2 wherein said step of determining includes determining a plurality nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
14 . The method of claim 13 wherein said plurality nucleotide at each of said nucleotide positions is a majority of nucleotides at such position.
15 . The method of claim 2 wherein said step of linearly amplifying is carried out by asymmetric PCR, NASBA or RCA.
16 . The method of claim 3 wherein said template or said nucleic acid is single stranded DNA.
17 . The method of claim 3 wherein said step of generating a plurality of sequence reads comprises separately amplifying each of said tag-template conjugates and sequencing each of the separately amplified tag-template conjugates to provide said sequence reads.
18 . The method of claim 17 wherein said step of separately amplifying is carried out by bridge PCR or emulsion PCR.
19 . The method of claim 3 wherein said step of determining includes determining a plurality nucleotide at each nucleotide position of each plurality of sequence reads having identical sequence tags.
20 . The method of claim 19 wherein said plurality nucleotide at each of said nucleotide positions is a majority of nucleotides at such position.