METHOD FOR ACCURATE QUANTIFICATION OF GENOMIC COPIES IN CELL-FREE DNA
Described herein are methods and systems for quantifying low molecular weight nucleic acid molecules in a biological sample amongst a background of high molecular weight contamination.
1 . A method for quantifying low molecular weight nucleic acid molecules in a biological sample comprising said low molecular weight nucleic acid molecules and high molecular weight nucleic acid molecules, comprising:
a. on a first subsample of said biological sample, quantifying total nucleic acid targets, wherein said total nucleic acids comprise both low molecular weight nucleic acid targets and high molecular weight nucleic acid targets;
b. on a second subsample of said biological sample, quantifying one or more high molecular weight nucleic acid targets, wherein said high molecular weight nucleic acid targets are longer than said low molecular weight nucleic acid targets; and
c. quantifying said low molecular weight nucleic acid targets in said biological sample by comparing an amount of said high molecular weight nucleic acid targets and said low molecular weight nucleic acid targets.
2 . The method of claim 1 , wherein said high molecular weight nucleic acid targets, said low molecular weight nucleic acid targets, or both comprise DNA molecules.
3 . The method of claim 1 or 2 , wherein digital PCR (dPCR) is used to quantify one or more of said high molecular weight nucleic acid targets, one or more of said low molecular weight nucleic acid targets, or both of said high molecular weight nucleic acid targets and said low molecular weight nucleic acid targets.
4 . The method of any one of claims 1 to 3 , wherein said low molecular weight nucleic acid targets are shorter than about 700 base pairs.
5 . The method of any one of claims 1 to 4 , wherein said low molecular weight nucleic acid targets are between about 150 to about 190 base pairs.
6 . The method of any one of claims 1 to 5 , wherein said high molecular weight nucleic acid targets are longer than about 700 base pairs.
7 . The method of any one of claims 1 to 6 , wherein said high molecular weight nucleic acid targets are between about 700 to about 2000 base pairs.
8 . The method of any one of claims 1 to 7 , wherein said low molecular weight DNA targets comprise cell-free DNA (cfDNA) present when said biological sample was obtained from an individual.
9 . The method of any one of claims 1 to 8 , wherein said high molecular weight DNA targets comprise genomic DNA inside a cell when said biological sample was obtained from an individual.
10 . The method of any one of claims 1 to 9 , wherein said low molecular weight nucleic acid targets are highly conserved regions of the genome.
11 . The method of any one of claims 1 to 10 , wherein said high molecular weight nucleic acid targets are highly conserved regions of the genome.
12 . The method of any one of claims 1 to 11 , wherein the average length of said low molecular weight nucleic acid targets is less than about 300 base pairs.
13 . The method of any one of claims 1 to 12 , wherein the average length of said low molecular weight nucleic acid targets is less than about 170 base pairs.
14 . The method of any one of claims 1 to 13 , wherein the average length of said high molecular weight nucleic acid targets is greater than about 300 base pairs.
15 . The method of any one of claims 1 to 14 , wherein the average length of said high molecular weight nucleic acid targets is greater than about 700 base pairs.
16 . The method of any one of claims 1 to 15 , wherein said low molecular weight nucleic acid targets comprise a plurality of low molecular weight nucleic acid targets selected to yield amplicons of different lengths across a genome.
17 . The method of any one of claims 1 to 16 , wherein said high molecular weight nucleic acid targets comprise a plurality of high molecular weight nucleic acid targets are selected to yield amplicons of different lengths across a genome.
18 . The method of any one of claims 1 to 17 , wherein said low molecular weight nucleic acid targets, said high molecular weight nucleic acid targets, or both said low molecular weight nucleic acid targets and said high molecular weight nucleic acid targets are quantified by a plurality of primer pairs that selectively hybridize to highly conserved regions of the genome.
19 . The method of any one of claims 1 to 18 , wherein said plurality of primer pairs used to quantify said low molecular weight nucleic acid targets are selected to yield at least two or more different length amplicons across at least two or more different target regions of the genome.
20 . The method of any one of claims 1 to 19 , wherein said plurality of primer pairs used to quantify said low molecular weight nucleic acid targets are selected to yield at least 7 different length amplicons across at least 4 different target regions of the genome.
21 . The method of any one of claims 1 to 20 , wherein said low molecular weight nucleic acid targets, said high molecular weight nucleic acid targets, or both said low molecular weight nucleic acid targets and said high molecular weight nucleic acid targets are quantified by a plurality of primer pairs that selectively hybridize to highly conserved regions of the genome.
22 . The method of any one of claims 1 to 21 , wherein the plurality of primer pairs to quantify the low molecular weight nucleic acid targets are selected to yield at least two or more different length amplicons across at least two or more different target regions of the genome.
23 . The method of any one of claims 1 to 22 , wherein the biological sample is selected from the list consisting of whole-blood, plasma, serum, saliva, lymph, and urine.
24 . A method for determining a conversion efficiency in one or more steps of a nucleic acid sequencing and analysis workflow, the method comprising:
a. performing a step of said nucleic acid sequencing and analysis workflow on a sample comprising low molecular weight nucleic acid targets and high molecular weight nucleic acid targets; and
b. quantifying, using a digital PCR (dPCR) amplification reaction, a number of said low molecular weight nucleic acid targets in said sample before and after said step of the sequencing and analysis workflow, and comparing the number of low molecular weight nucleic acid targets in the sample before and after said sequencing and analysis workflow to determine said conversion efficiency of the step.
25 . The method of claim 24 , wherein said dPCR amplification reaction comprises droplet digital polymerase chain (ddPCR).
26 . The method of claim 24 or 25 , wherein said one or more steps of said sequencing and analysis workflow is selected from the group consisting of: DNA isolation, enrichment, ligating adaptors, performing a universal amplification step, attaching barcodes, and sequencing.
27 . The method of any one of claims 24 to 26 , wherein said step of said sequencing and analysis workflow is a plurality of steps selected from the group consisting of: DNA isolation, enrichment, ligating adaptors, performing a universal amplification step, attaching barcodes, and sequencing.
28 . The method of any one of claims 24 to 27 , wherein said low molecular weight nucleic acid targets are quantified by a plurality of primer pairs that selectively hybridize to highly conserved regions of the genome.
29 . The method of claim 24 , wherein quantifying comprises determining a first target count using a first set of one or more primer pairs that amplify one or more first regions of the genome and a second target count using a second set of one or more primer pairs that amplify one or more second regions of the genome.
30 . The method of any one of claims 24 to 28 , wherein estimating the conversion efficiency comprises comparing the second target count and the first target count.
31 . The method of any one of claims 24 to 29 , wherein the step is repeated if said conversion efficiency is less than about 20%.
32 . The method of any one of claims 24 to 31 , wherein the average length of said low molecular weight nucleic acid targets are is less than about 300 base pairs.
33 . The method of any one of claims 24 to 32 , wherein the average length of said low molecular weight nucleic acid targets is less than about 170 base pairs.