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Next Generation Sequencing Platforms

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All numbers and specifications as of November 2011 - please check the Wiki page for latest information and updates !

  Applications Specifications Input Material
Life Technologies 5500xl


SAGE/small RNA

Whole transcriptome

ChIP-seq

Methylation

Whole genome resequencing

Targeted resequencing

Throughput: 150 Mio reads/lane
up to: 2 Gigabases per run

Read-length:
  Fragment: 75 bp
  Mate-pair: 2 x 60 bp
  Paired-end: 75 + 35 bp

Parallel and independent processing of up to 12 lanes. Multiple applications can be processed within the same run.

Barcodes available for the parallel measurement (multiplexing) of up to 96 samples

DNA Fragment library -  500ng of high quality column purified genomic DNA

Mate Pair library-  5-20µg of high quality column purified genomic DNA

Targeted Enrichment (Sure Select) - 3µg of high quality column purified genomic DNA

Chip-Seq - 20ng-1µg DNA

RNA seq -  200ng of poly(A) RNA or 200ng of rRNA-depleted RNA

small RNA analysis - 5-10µg of integral  high quality total RNA

 Pacific  Biosciences  RS Backbone  sequecning

de novo sequencing

Methylation studies
Throughput: 40 000 reads

Read length: Average ~1500 bp, individual reads up to 10000 bp

500bp library - 1µg of high quality column purified genomic DNA

2000bp library - 3µg of  high quality column purified genomic DNA

8000bp library - 8µg of  high quality column purified genomic DNA

1 library prep. produces enough material to sequence at least 2 SMRT cells

 Illumina HiSeq 2000
SAGE/small RNA

Whole transcriptome

de novo sequencing

ChIP-seq

Methylation

Whole genome resequencing

Targeted resequencing

Throughput: 3000 Mio reads
up to 600 Gigabases per run

Read length: 2 X 100 bp

DNA Seq - From 1 μg high-quality

RNA-free genomic DNA

RNA Seq - From 100 ng to 4 µg column purified, genomic DNA free total RNA

Small RNA Seq - From 1 to 10 μg of trizol purified total RNA

Chip Seq -From 10 ng Single ChIP enriched DNA or input DNA
 Ion Torrent PGM
Amplicon sequencing

Small genome sequencing

Small RNA
Throughput:
> 10 Megabases (314 chip)
> 100 Megabases (316 chip)

Read length: 200 bp
DNA Seq - From 100 ng to 5 μg high-quality RNA-free genomic DNA

RNA Seq - From 200 ng to 1 µg poly(A)RNA or rRNA-depleted total RNA
Roche 454 GS FLX+


de novo genome sequencing

de novo transcriptome sequencing

Whole genome resequencing

Fragment/amplicon deep sequencing

Over 1 Million reads per run
up to 700 Million bases per instrument run


Average read length of 700 bases
Maximum read length of 1000 bases


single read accuracy greater than 99.5%
consensus accuracy greater than 99.99%

1ug for an average read length of 700bp

500ng for a shotgun fragment library of 400bp read-length

For mate pair libraries, with insert sizes of 3 kb, 8kb or 20kb, we need a input of gDNA of 5ug, 15ug or 30ug, respectively.

For RNA analysis, 1 to 2 ug of total RNA.

E-mail contact: sequencing@fgcz.ethz.ch

 

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© 2012 FGCZ Zurich | Imprint | Disclaimer | 4 November 2011
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