Methods of sequencing nucleic acids and error correction of sequence reads
AssigneeInivata Ltd.
InventorsSamuel WOODHOUSE, Tim FORSHEW, Stefanie Viola LENSING
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AssigneeInivata Ltd.
InventorsSamuel WOODHOUSE, Tim FORSHEW, Stefanie Viola LENSING
Estimating the term…
Described herein, among other things, is a method of sequencing nucleic acids of interest (NAOIs). In some embodiments the method may comprise: providing a sample comprising NAOIs; attaching oligonucleotides to the NAOIs to provide labelled NAOIs, wherein the oligonucleotides comprise a PCR cycle counter generator sequence comprising at least one universal nucleotide base; amplifying the labelled NAOIs using PCR to provide an amplified library of NAOIs each containing a PCR cycle counter sequence; sequencing the amplified library of NAOIs to provide a set of sequence reads, wherein each sequence read comprises a NAOI-originating component and a PCR cycle counter component; and distinguishing true variants in NAOI sequences from false variants in NAOI sequences.
A method of sequencing nucleic acids of interest (NAOIs), comprising:
A double-stranded oligonucleotide comprising a first and a second strand, the first strand comprising a PCR cycle counter generator sequence comprising one or more universal bases and a 3′ ligation moiety, and the second strand comprising a region complementary to the PCR cycle counter generator sequence and a 5′ ligation moiety.
18-33. (canceled)
36-39. (canceled)
Dependencies are inferred from the claim text.