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The Genome Assemblies The Genome Assemblies of of
Tasmanian Devil
Zemin NingZemin Ning
The Wellcome Trust Sanger InstituteThe Wellcome Trust Sanger Institute
The Phusion2 pipeline Flow-sorting sequencing Assigning contigs to individual chromosomes The Devil genome assembly Future work
Outline of the Talk:
Phusion2 Assembly PipelinePhusion2 Assembly Pipeline
SolexaReads
Assembly
Reads Group
Data Process Long Insert Reads
Supercontig
Contigs
PRono
Fuzzypath
Velvet
Phrap
2x75 or 2x100
BaseCorrection
GraphRP
Mis-assembly Errors: Mis-assembly Errors: Contig Break based Contig Break based
on Inconsistent Pairson Inconsistent Pairs
Mis-assembly Errors: Mis-assembly Errors: Contig Break Based on Pair CoverageContig Break Based on Pair Coverage
Pipeline of Contig Gap ClosurePipeline of Contig Gap Closure
Sequencing T. Devil on Illumina: Strategy
Tumour or normal genomic DNA
Fragments of defined size0.5, 2, 5, 7, 8, 10 kb
Sequencing
2x100bp reads short insert
2x50bp mate pairs
Alignment using bwa, smalt
Somatic mutations
Germline variants
fragment size distribution
0
20000
40000
60000
80000
100000
120000
140000
160000
180000
0 1000 2000 3000 4000 5000 6000
size
fre
qu
en
cy
tumour 2kb
tumour 3kb
tumour 4kb
normal 2kb
normal 3kb
normal 4kb
Sequencing performed at Illumina
De novo Assembly
Table 1 Run ID, Template names, Number of reads and Chromosome size4972_1 chr1 IL20_4972:1 19.8 5714967_1 chr2 IL21_4967:1 20.0 6104971_1 chr3 IL30_4971:1 21.7 5564964_1 chr4 IL14_4964:1 7.26 4504969_1 chr5 IL17_4969:1 7.06 3414969_2 chr6 IL17_4969:2 8.59 2774969_3 chrx IL17_4969:3 9.43 122
Read mapping coefficient:Read mapping coefficient:
e = Size_of_Chr/Num_reads_in_lanee = Size_of_Chr/Num_reads_in_lane
Chr1 EAS25_101_1 70 549Chr1 EAS25_101_2 70 549
Chr2 EAS25_101_3 70 580Chr2 EAS25_101_4 70 580
Chr3 EAS25_101_5 70 547Chr3 EAS25_101_6 70 547
Chr4 EAS188_173_3 70 448Chr4 EAS188_173_4 70 448
Chr5 EAS188_173_5 70 346Chr5 EAS188_173_6 70 346
Chr6 EAS188_173_7 70 285Chr6 EAS188_173_8 70 285
Chrx EAS188_173_2 70 122
New Data Sequenced by IlluminaNew Data Sequenced by Illumina
Table 2 Chr_ID, Chr_size, Contigs_assigned Bases_assigned N_reads
Chr1 571 65262 604 19.8Chr2 610 76959 673 20.0Chr3 556 68842 585 21.7Chr4 450 48352 446 7.26Chr5 341 30451 279 7.06Chr6 277 25726 250 8.59Chrx 122 14189 83.6 9.53Unassigned 60841 54.7 (1.8%)
Table 2 Chr_ID, Chr_size, Contigs_assigned Bases_assigned Mb
Chr1 571 6729 684 Chr2 610 8381 740 Chr3 556 7197 641Chr4 450 4817 487Chr5 341 3188 300 Chr6 277 2844 263Chrx 122 2378 86.6Unassigned 440 1.23
New Data Sequenced by IlluminaNew Data Sequenced by Illumina
Unassigned contigs were placed by Unassigned contigs were placed by supercontigs using mate pairssupercontigs using mate pairs
Solexa reads:Number of read pairs: 650 Million;Finished genome size: 3.3 GB;Read length: 2x100bp;Estimated read coverage: ~40X;Insert size: 410/50-600 bp;Mate pair data: 2k,4k,5k,6k,8k,10kNumber of reads clustered: 591 Million
Assembly features: - statsContigs Supercontigs
Total number of contigs: 237,291 35,974Total bases of contigs: 2.93 Gb 3.17 GbN50 contig size: 20,139 1,847,186Largest contig: 189,866 5,315,556 Averaged contig size: 12,354 88,254Contig coverage on genome: ~94% >99%Ratio of placed PE reads: ~92% ?
Genome Genome Assembly Normal – T. DevilAssembly Normal – T. Devil
Acknowledgements:
Elizabeth Murchuson David McBride Fengtang Yang Mike Stratton
Ole Schulz-Trieglaff Dirk Evers David Bentley