Single cell analysis of transposase accessible chromatin
Methods and systems for sample preparation techniques that allow amplification (e.g., whole genome amplification) and sequencing of chromatin accessible regions of single cells are provided. The methods and systems generally operate by forming or providing partitions (e.g., droplets) including a single biological particle and a single bead comprising a barcoded oligonucleotide. The preparation of barcoded next-generation sequencing libraries prepared from a single cell is facilitated by the transposon-mediated transposition and fragmentation of a target nucleic acid sequence. The methods and systems may be configured to allow the implementation of single-operation or multi-operation chemical and/or biochemical processing within the partitions.
1. A system for nucleic acid processing of multiple cells or cell nuclei that enables analysis of DNA originating from an individual cell or cell nucleus, comprising:
(a) a transposase-nucleic acid complex comprising a transposase enzyme and a nucleic acid molecule comprising an adapter sequence, wherein said transposase-nucleic acid complex is capable of generating a plurality of adapter-flanked nucleic acid fragments in a plurality of cells or cell nuclei;
(b) a microfluidic device comprising a receiving component that receives said plurality of cells or cell nuclei, wherein a cell or cell nucleus of said plurality of cells or cell nuclei comprises at least one adapter-flanked nucleic acid fragment of said plurality of adapter-flanked nucleic acid fragments, wherein each said adapter-flanked nucleic acid fragment is indicative of a region of accessible chromatin within said cell or cell nucleus, and a channel structure that partitions (i) said plurality of cells or cell nuclei; and (ii) a plurality of barcoded beads into a plurality of droplets,
wherein said plurality of barcoded beads comprises a plurality of nucleic acid molecules comprising barcode sequences,
wherein a droplet of said plurality of droplets comprises:
(1) a cell or cell nucleus of said plurality of cells or cell nuclei comprising said at least one adapter-flanked nucleic acid fragment, and
(2) a barcoded bead of said plurality of barcoded beads, wherein said barcoded bead comprises nucleic acid molecules comprising a common barcode sequence,
wherein said common barcode sequence of said nucleic acid molecules of said barcoded bead differs from nucleic acid barcode sequences of other barcoded beads in other droplets of said plurality of droplets; and
wherein said system is capable of generating a barcoded, adapter-flanked nucleic acid fragment comprising said common barcode sequence.
2. The system of claim 1 , wherein said barcoded bead is a barcoded gel bead.
3. The system of claim 2 , wherein said barcoded gel bead comprises a labile bond, and wherein a droplet of said plurality of droplets comprises a chemical agent capable of breaking said labile bond, thereby degrading said barcoded gel bead.
4. The system of claim 1 , wherein said nucleic acid molecules comprising said common barcode sequence further comprise a sequence complementary to said adapter sequence.
5. The system of claim 4 , further comprising a ligation component comprising a ligase enzyme, wherein said ligation component is capable of ligating a nucleic acid molecule comprising said common barcode sequence to said adapter-flanked nucleic acid fragment to generate said barcoded, adapter-flanked nucleic acid fragment.
6. The system of claim 4 , further comprising an amplification component comprising a polymerase enzyme, wherein said amplification component is capable of using a nucleic acid molecule comprising said common barcode sequence and said adapter-flanked nucleic acid fragment to generate said barcoded, adapter-flanked nucleic acid fragment.
7. The system of claim 1 , wherein said plurality of cells or cell nuclei is a plurality of cell nuclei.
8. The system of claim 7 , further comprising a permeabilization component comprising a buffer and a lysis reagent, wherein said permeabilization component is capable of permeabilizing said plurality cell nuclei.
9. The system of claim 1 , wherein said transposase-nucleic acid complex comprises a transposase dimer comprising (i) a first transposase monomer bound to a first nucleic acid molecule comprising a first adapter sequence, and (ii) a second transposase monomer bound to a second nucleic acid molecule comprising a second adapter sequence, wherein said first adapter sequence is different than said second adapter sequence, and wherein said adapter-flanked nucleic acid fragment is flanked by said first adapter sequence and said second adapter sequence.
10. The system of claim 9 , wherein said first adapter sequence comprises a first sequencing primer sequence, wherein said second adapter sequence comprises a second sequencing primer sequence, and wherein said first sequencing primer sequence is a different sequence than said second sequencing primer sequence.
11. The system of claim 9 , wherein said nucleic acid molecules comprising said common barcode sequence further comprise a sequence complementary to said first adapter sequence.
12. The system of claim 11 , wherein said nucleic acid molecules comprising said common barcode sequence further comprise a first flow-cell adapter sequence capable of attaching to a flow cell of a sequencer.
13. The system of claim 12 , further comprising an amplification component comprising a buffer, a DNA polymerase, a first primer complementary to said first flow-cell adapter sequence, and a second primer complementary to said second adapter sequence, wherein said second primer comprises a second flow-cell adapter sequence capable of attaching to the flow cell of a sequencer, and wherein said amplification component is capable of generating a sequencing library.
14. The system of claim 13 , wherein said second primer further comprises a sample index sequence.
15. The system of claim 1 , further comprising a sequencing component comprising a sequencing instrument capable of generating a plurality of sequencing reads corresponding to said adapter-flanked nucleic acid fragment.
16. The system of claim 15 , further comprising a computing component comprising a processor, a user interface, and an electronic display, wherein said computing component is capable of analyzing said sequencing reads and displaying an analysis of nucleic acid sequencing data on said electronic display.
17. The system of claim 16 , wherein said analysis comprises a representation of accessible chromatin of said cell or cell nucleus.
18. The system of claim 1 , wherein said barcoded bead comprises a labile bond, and wherein said partition further comprises an agent capable of breaking said labile bond, thereby releasing and removing said nucleic acid molecules comprising said common barcode sequence from said barcoded bead.
19. The system of claim 18 , wherein said agent is a chemical agent.
20. A system for nucleic acid processing of multiple cells or cell nuclei that enables analysis of DNA originating from an individual cell or cell nucleus, comprising:
(a) a transposase-nucleic acid complex comprising a transposase enzyme and a nucleic acid molecule comprising an adapter sequence, wherein said transposase-nucleic acid complex is capable of generating a plurality of adapter-flanked nucleic acid fragments in a plurality of cells or cell nuclei;
(b) a device comprising 1,000 wells that is capable of receiving said plurality of cells or cell nuclei, wherein a cell or cell nucleus of said plurality of cells or cell nuclei comprises at least one adapter-flanked nucleic acid fragment of said plurality of adapter-flanked nucleic acid fragments, wherein each said adapter-flanked nucleic acid fragment is indicative of a region of accessible chromatin within said cell or cell nucleus, and wherein said device partitions (i) said plurality of cells or cell nuclei; and (ii) a plurality of barcoded beads into wells of said 1,000 wells,
wherein said plurality of barcoded beads comprises a plurality of nucleic acid molecules comprising barcode sequences,
wherein a well of said 1,000 wells comprises:
(1) a cell or cell nucleus of said plurality of cells or cell nuclei comprising said at least one adapter-flanked nucleic acid fragment, and
(2) a barcoded bead of said plurality of barcoded beads, wherein said barcoded bead comprises nucleic acid molecules comprising a common barcode sequence,
wherein said common barcode sequence of said nucleic acid molecules of said barcoded bead differs from nucleic acid barcode sequences of other barcoded beads in other wells of said 1,000 wells; and
wherein said system is capable of generating a barcoded, adapter-flanked nucleic acid fragment comprising said common barcode sequence.
21. The system of claim 20 , wherein said barcoded bead comprises a labile bond, and wherein said well further comprises an agent capable of breaking said labile bond, thereby releasing and removing said nucleic acid molecules comprising said common barcode sequence from said barcoded bead.
22. The system of claim 21 , wherein said nucleic acid molecules comprising said common barcode sequence further comprise a sequence complementary to said adapter sequence.
23. The system of claim 22 , further comprising a ligation component comprising a ligase enzyme, wherein said ligation component is capable of ligating a nucleic acid molecule comprising said common barcode sequence to said adapter-flanked nucleic acid fragment to generate said barcoded, adapter-flanked nucleic acid fragment.
24. The system of claim 22 , further comprising an amplification component comprising a polymerase enzyme, wherein said amplification component is capable of using a nucleic acid molecule comprising said common barcode sequence and said adapter-flanked nucleic acid fragment to generate said barcoded, adapter-flanked nucleic acid fragment.
25. The system of claim 22 , wherein said transposase-nucleic acid complex comprises a transposase dimer comprising (i) a first transposase monomer bound to a first nucleic acid molecule comprising a first adapter sequence, and (ii) a second transposase monomer bound to a second nucleic acid molecule comprising a second adapter sequence, wherein said first adapter sequence is different than said second adapter sequence, and wherein said adapter-flanked nucleic acid fragment is flanked by said first adapter sequence and said second adapter sequence.
26. The system of claim 25 , wherein said first adapter sequence comprises a first sequencing primer sequence, wherein said second adapter sequence comprises a second sequencing primer sequence, and wherein said first sequencing primer sequence is a different sequence than said second sequencing primer sequence.
27. The system of claim 25 , wherein said nucleic acid molecules comprising said common barcode sequence further comprise a sequence complementary to said first adapter sequence.
28. The system of claim 27 , wherein said nucleic acid molecules comprising said common barcode sequence further comprise a first flow-cell adapter sequence capable of attaching to a flow cell of a sequencer.
29. The system of claim 28 , further comprising an amplification component comprising a buffer, a DNA polymerase, a first primer complementary to said first flow-cell adapter sequence, and a second primer complementary to said second adapter sequence, wherein said second primer comprises a second flow-cell adapter sequence capable of attaching to the flow cell of a sequencer, and wherein said amplification component is capable of generating a sequencing library.
30. The system of claim 29 , wherein said second primer further comprises a sample index sequence.