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Table 1 Summary of massively parallel sequencing technologies

From: Next-generation sequencing

Method

Amplification

Read length (base pairs)

Templates per run

Data production/day

Sequence reaction

Reference

Commercially available technologies

   ABI 3730xI

PCR

~900 to 1,100

96

1 Mb/day

Sanger method

http://www.appliedbyosystems.com

   454 FLX Roche

Emulsion PCR

~400

1,000,000

400 Mb/run/7.5 to 8 hours

Pyrosequencing

http://www.rocheapplied-science.com

   Illumina (Solexa) Genome Analyzer

Bridge PCR

36 to 175

40,000,000

>17 Gb/run/3 to 6 days

Reverse terminator

http://www.illumina.com

   ABI SOLiD

Emulsion PCR

~50

85,000,000

10 to 15 Gb/run/6 days

Ligation sequencing

http://www.appliedbyosystems.com

   Helicos Heliscope

None

30 to 35

800,000,000

21 to 28 Gb/run/8 days

Single molecule sequence by synthesis

http://www.helicosbio.com

Technologies in development

   Pacific Biosciences

None

>1,000

NA

NA

Single molecule real-time DNA sequencing

http://www.pacificbiosciences.com

   Intelligent Biosciences

Yesa

NA

NA

NA

Sequence by synthesis

http://www.intelligentbiosystems.com

   Visigen Biotechnologies

None

NA

NA

NA

Base-specific FRET emission

http://www.visigenbio.com

   ZS Genetics

None

NA

NA

NA

ZSG atomic labelling and electron microscopy

http://www.zsgenetics.com

  1. NA, not available at present. aAmplification method not yet standardised. FRET, Förster resonance energy transfer.