IP Library › Patent Application 15014642
Patent Application
App. No. 15/014,642

METHOD FOR GENOME SEQUENCING USING A SEQUENCE-BASED PHYSICAL MAP

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Patent No.
US None
App. No.
15/014,642
Abstract

The present invention relates to a high throughput method for the identification and detection of molecular markers wherein restriction fragments are generated and suitable adaptors comprising (sample-specific) identifiers are ligated. The adapter-ligated restriction fragments may be selectively amplified with adaptor compatible primers carrying selective nucleotides at their 3′ end. The amplified adapter-ligated restriction fragments are, at least partly, sequenced using high throughput sequencing methods and the sequence parts of the restriction fragments together with the sample-specific identifiers serve as molecular markers.

Claims (40)

1 . A method for the generation of a physical map of at least part of a genome comprising the steps of:

(a) generating an artificial chromosome clone bank wherein each artificial chromosome clone contains part of a sample DNA;

(b) combining the artificial chromosome clones in one or more pools, wherein each clone is present in more than one pool, to create a library;

(c) digesting the one or more pools with one or more restriction endonucleases to provide restriction fragments for each pool;

(d) ligating adaptors to one or both sides of the restriction fragments, wherein at least one adaptor contains a pool-specific identifier or a degenerate identifier section to provide adaptor-ligated restriction fragments;

(e) optionally, combining the adaptor-ligated restriction fragments;

(f) amplifying the adaptor-ligated restriction fragments of step (d) with at least one primer, which primer contains a pool-specific section corresponding to the pool-specific identifier section in the adaptor or contains a pool-specific identifier at the position of the degenerate identifier section, respectively, to provide amplified adaptor-ligated restriction fragments (amplicons);

(g) optionally, combining the amplicons in a set of combined amplicons;

(h) determining the sequence of at least the pool-specific identifier and part of the restriction fragment of the amplicons or set of combined amplicons;

(i) assigning the restriction fragment sequences determined in the amplicons of step (h) to the corresponding clones using the pool-specific identifiers;

(j) ordering the restriction fragments derived from the same clone to build a contig;

(k) ordering the contigs of the clones of step (j) to thereby build a clone-contig and generate a physical map.

2 . The method according to claim 1 , wherein the restriction fragments are assigned to the corresponding clone by clustering amplicons that contain identical sequences in the restriction fragments but carry different pool-specific identifiers.

3 . The method according to claim 1 , wherein the sequencing is carried out by means of high-throughput sequencing.

4 . The method according to claim 3 , wherein the high-throughput sequencing is performed on a solid support.

5 . The method according to claim 3 , wherein the high-throughput sequencing is based on Sequencing-by-Synthesis.

6 . The method according to claim 3 , wherein the high-throughput sequencing comprises the steps of:

annealing the amplicons or adapter-ligated restriction fragments to beads, each bead annealing with a single adapter-ligated restriction fragments or amplicon;

emulsifying the beads in water-in-oil micro reactors, each water-in-oil micro reactor comprising a single bead;

performing emulsion PCR to amplify adapter-ligated restriction fragments or amplicons on the surface of beads,

optionally, selecting and enriching beads containing amplified amplicons;

loading the beads in wells, each well comprising a single bead; and

generating a pyrophosphate signal.

7 . The method according to claim 3 , wherein the high-throughput sequencing comprises the steps of:

annealing the adapter-ligated restriction fragments or amplicons to a surface containing first and second primers or first and second primer binding sequences respectively,

performing bridge amplification to provide clusters of amplified adapter-ligated restriction fragments or amplified amplicons,

determining the nucleotide sequence of the amplified adapter-ligated restriction fragments or amplified amplicons using labelled reversible terminator nucleotides.

8 . The method according to claim 1 , wherein the identifier is from 4-16 bp.

9 . The method according to claim 8 , wherein the identifier does not contain 2 or more identical consecutive bases.

10 . The method according to claim 8 , wherein for two or more clones, the corresponding identifiers contain at least two different nucleotides.

11 . The method according to claim 1 , wherein the at least one primer carries 1-10 selective nucleotides at it 3′ end to provide for a random subset of amplicons.

12 . A kit comprising one or more primers as defined in claim 1 .

13 . A kit comprising one or more adaptors as defined in claim 1 .

14 . A kit comprising primers and adaptors as defined in claim 1 .

15 . A method for identifying the clonal source of a restriction fragment, comprising:

(a) digesting artificial chromosome clones in a plurality of pools with one or more restriction endonucleases to provide for a set of restriction fragments for each pool, and wherein each clone is present in more than one pool;

(b) ligating adaptors to one or both sides of the restriction fragments, wherein at least one adaptor contains a pool-specific identifier or a degenerate identifier section, respectively, to provide adaptor-ligated restriction fragments;

(c) sequencing at least the pool-specific identifier and part of the restriction fragment; and

(d) assigning the restriction fragment sequences of step (c) to the corresponding clonal sources using the pool-specific identifiers.

16 . A kit comprising one or more adaptors as defined in claim 15 .