Assay systems for determination of fetal copy number variation
The present invention provides processes for determining accurate risk probabilities for chromosome dosage abnormalities. Specifically, the invention provides non-invasive evaluation of genomic variations through chromosome-selective sequencing and non-host fraction data analysis of maternal samples.
1. A method for determining a likelihood of the presence or absence of a copy number variation (CNV) in a fetal genomic region in a maternal sample from a pregnant female, comprising:
a) obtaining the maternal sample from the pregnant female, the maternal sample comprising a fetal source and a maternal source;
b) executing, by a CNV processing system, a process for determining the likelihood of the presence or absence of CNV in the fetal genomic region, the process comprising the following steps:
1) interrogating at least twenty polymorphic loci in a first fetal genomic region in the maternal sample and interrogating at least twenty polymorphic loci in a second fetal genomic region of the maternal sample;
2) determining fetal DNA contribution to the maternal sample;
3) calculating an estimated dosage of the first fetal genomic region in the maternal sample and calculating an estimated dosage of at least the second fetal genomic region in the maternal sample; and
4) comparing the estimated dosages of the first and second fetal genomic regions to determine the likelihood of the presence or absence of the CNV in the first fetal genomic region in view of the fetal DNA contribution to the maternal sample; and
c) assisting in a communication of the determined likelihood of the presence or absence of the CNV in the first fetal genomic region to the pregnant female.
2. The process of claim 1 , wherein the maternal sample is a cell free maternal sample.
3. The process of claim 2 , wherein the cell free maternal sample is maternal plasma or serum.
4. The process of claim 1 , wherein the copy number variation is a chromosomal aneuploidy, and wherein the calculated contributions measure fetal chromosome dosage.
5. The process of claim 1 , wherein the presence or absence of a copy number variation of the first genomic region is estimated by interrogating at least fifty polymorphic loci in the first and second genomic regions.
6. The process of claim 1 , wherein the presence or absence of a copy number variation is estimated by interrogating at least five informative loci in the first and second genomic regions.
7. The process of claim 1 , wherein the presence or absence of a copy number variation is estimated by interrogating at least twenty informative loci in the first and second genomic regions.
8. A method to calculate a risk of a fetal aneuploidy in a maternal serum or plasma sample from a pregnant female comprising:
a) obtaining the maternal sample from the pregnant female, the maternal sample comprising a fetal source and a maternal source;
b) executing, by a fetal aneuploidy processing system, a process comprising the following steps:
i. interrogating at least twenty polymorphic loci on a first fetal chromosome in the maternal sample and interrogating at least twenty polymorphic on a second fetal chromosome in the maternal sample;
ii. identifying genetic loci contributed to a fetus from non-maternal sources;
iii. determining fetal DNA contribution to the maternal sample;
iv. determining a relative number of copies of the first fetal chromosome in the maternal sample;
v. estimating the chromosome dosage of the first fetal chromosome in the maternal sample using the determined relative number of copies;
vi. determining a relative number of copies of the second fetal chromosome in the maternal sample;
vii. estimating the chromosome dosage of the second fetal chromosome in the maternal sample using the determined relative number of copies;
viii. calculating a value of the likelihood that a first fetal chromosome is aneuploid by constructing an aneuploid model by comparing the estimated chromosome dosage of the first fetal chromosome to the estimated chromosome dosage of the second fetal chromosome in view of the fetal DNA contribution to the maternal sample;
ix. calculating a value of the likelihood that the first fetal chromosome is disomic by constructing a disomic model by comparing the estimated chromosome dosage of the first fetal chromosome to the estimated chromosome dosage of the second fetal chromosome; and
x. providing a calculated risk of aneuploidy of the first fetal chromosome based on the calculated values of likelihood that the first fetal chromosome is aneuploid and the first fetal chromosome is disomic using an odds ratio comparing the model assuming a disomic first fetal chromosome and the model assuming an aneuploid first fetal chromosome adjusted by a prior risk of trisomy and disomy; and
c) assisting in a communication of the calculated risk of aneuploidy of the first fetal chromosome to the pregnant female.
9. The process of claim 8 , wherein the maternal sample comprises cells.
10. The process of claim 8 , wherein the chromosome dosage of the first chromosome is estimated by interrogating at least fifty polymorphic loci on the first chromosome.
11. The process of claim 8 , wherein the chromosome dosage of the first chromosome is estimated by interrogating at least five informative loci on the first chromosome.
12. The process of claim 11 , wherein the chromosome dosage of the first chromosome is estimated by interrogating at least twenty informative loci on the first chromosome.
13. The process of claim 8 , wherein the value of the probability of an aneuploidy is an odds ratio.
14. The process of claim 8 , wherein the risk of aneuploidy of the first fetal chromosome is based on a value of the likelihood of the first fetal chromosome being trisomic and the value of the likelihood of the first fetal chromosome being disomic.
15. The process of claim 8 , wherein the value of the probability of a chromosome dosage abnormality for the first fetal chromosome is based on a value of the likelihood of the chromosome being monosomic and a value of the likelihood of the chromosome being disomic.
16. The process of claim 8 , wherein the determining the fetal DNA contribution to the maternal sample step is accomplished by quantifying SNPs using multiplexed SNP detection without prior knowledge of maternal or paternal genotype.
17. The process of claim 8 , wherein the determining the fetal DNA contribution to the maternal sample step is accomplished by quantifying SNPs where maternal and fetal genotypes are different.
18. The process of claim 8 , wherein the determining the fetal DNA contribution to the maternal sample step is accomplished by epigenetic differences between the fetus and mother.