Digital analyte analysis
The invention generally relates to droplet based digital PCR and methods for analyzing a target nucleic acid using the same. In certain embodiments, a method for determining the nucleic acid make-up of a sample is provided.
1. A method comprising:
partitioning a first sample fluid comprising nucleic acid molecules obtained from a single cell into a plurality of fluid partitions, wherein a plurality of the fluid partitions each contain one nucleic acid molecule;
merging the fluid partitions with a second sample fluid comprising amplification reagents;
performing an amplification reaction in the plurality of fluid partitions using first primers that include 5′ tail regions; and
performing a second amplification reaction using a second primers that anneals to the 5′ tail regions of the first primers, wherein the second primers include second tail sequences that include barcode sequences, to produce amplicons comprising the barcode sequences and copies of the nucleic acid.
2. The method of claim 1 , wherein the amplification reactions use primers that further include at least one sequencing adaptor.
3. The method of claim 2 , further comprising preparing a sequencing library comprising adaptor-containing amplicons.
4. The method of claim 2 , further comprising sequencing the amplicons.
5. The method of claim 1 , further comprising pooling barcoded amplicons and performing a multiplexed reaction.
6. The method of claim 5 , wherein the multiplexed reaction includes sequencing the pooled, barcoded amplicons.
7. The method of claim 1 , wherein the second tail sequence comprises a linked molecule for separation of the amplicons from the sample, wherein the molecule for separation optionally include one selected from the group consisting of biotin, digoxin, streptavidin, peptides, and antibodies.
8. The method of claim 1 , wherein the fluid partitions comprise aqueous droplets.