METHOD FOR SAMPLE ANALYSIS OF ANEUPLOIDIES IN MATERNAL SAMPLES
The invention provides methods for determining aneuploidy and/or fetal fraction in maternal samples comprising fetal and maternal cfDNA by massively parallel sequencing. The method comprises a novel protocol for preparing sequencing libraries that unexpectedly improves the quality of library DNA while expediting the process of analysis of samples for prenatal diagnoses. The novel protocol can be performed in solution or on a solid surface.
1 . A method for determining the presence or absence of one or more fetal chromosomal aneuploidies, said method comprising:
(a) obtaining a maternal sample comprising a mixture of fetal and maternal cell-free DNA (cfDNA);
(b) isolating said mixture of fetal and maternal cfDNA from said sample;
(c) preparing a sequencing library from said mixture of fetal and maternal cfDNA; wherein preparing said library comprises the consecutive steps of dA-tailing and adaptor ligating said cfDNA, and wherein said preparing excludes end-repairing said cfDNA;
(d) massively parallel sequencing at least a portion of said sequencing library to obtain sequence information for said fetal and maternal cfDNA in said sample;
(e) storing in a computer readable medium, at least temporarily, said sequence information;
(f) using said stored sequence information to computationally identify a number of sequence tags for each of said one or more chromosomes of interest and for a normalizing sequence for each of said any one or more chromosome of interest;
(g) computationally calculating, using said number of sequence tags for each of said one or more chromosomes of interest and the number of sequence tags for said normalizing sequence for each of said one or more chromosomes of interest, a chromosome dose for each of said one or more chromosomes of interest; and
(h) comparing said chromosome dose for each of said one or more chromosomes of interest to a corresponding threshold value for each of said one or more chromosomes of interest, and thereby determining the presence or absence of said fetal chromosomal aneuploidy in said sample, wherein steps (e)-(g) are performed using one or more processors.
2 . The method of claim 1 , wherein the step of preparing said sequencing library is performed in solution.
3 . The method of claim 1 , wherein the step of preparing said library is performed on a solid phase.
4 . The method of claim 3 , wherein said preparing said library on a solid phase further comprises the consecutive step of amplifying the adaptor-ligated cfDNA.
5 . The method of claim 1 , wherein said consecutive steps are performed in the absence of polyethylene glycol.
6 . The method of claim 1 , wherein step (g) comprises computationally calculating a chromosome dose for a elected one of said chromosome of interest as a ratio of the number of sequence tags identified for said selected chromosome of interest and the number of sequence tags identified for a corresponding normalizing sequence for the selected chromosome of interest.
7 . The method of claim 1 , wherein said adaptor comprises an index sequence.
8 . The method of claim 1 , wherein said consecutive steps exclude purification.
9 . The method of claim 1 , wherein said each of said one or more chromosomes of interest is selected from chromosomes 1-22, X, and Y.
10 . The method of claim 1 , wherein said fetal chromosomal aneuploidies are selected from trisomy 2, trisomy 8, trisomy 9, trisomy 13, trisomy 16, trisomy 18, trisomy 21, trisomy 22, 47,XXY, 47,XXX, 47,XYY, and monosomy X.
11 . The method of claim 1 , wherein said normalizing sequence is a single chromosome or a group of chromosomes.
12 . The method of claim 1 , wherein said normalizing sequence is a single chromosome segment or a group of chromosome segments.
13 . The method of claim 1 , wherein said massively parallel sequencing is sequencing-by-synthesis using reversible dye terminators.
14 . The method of claim 1 , wherein said massively parallel sequencing is sequencing by ligation.
15 . The method of claim 1 , wherein said massively parallel sequencing is single molecule sequencing.
16 . The method of claim 1 , wherein said maternal sample is a biological fluid sample.
17 . The method of claim 1 , wherein said maternal sample is a blood sample, a plasma sample, a serum sample, or a urine sample.
18 . The method of claim 1 , wherein said massively parallel sequencing comprises as solid phase amplification.