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Cheatography

Short Reads Sequencing Technologies Cheat Sheet (DRAFT) by

Comparing 3 short read sequencing technologies

This is a draft cheat sheet. It is a work in progress and is not finished yet.

Signal Amplif­ication

Illumina
MGI
Element Bio
Bridge amplif­ication
Rolling Circle Amplif­ication (RCA)
Rolling Circle Amplif­ication (RCA)
PCR
NO error propag­ation by PCR
NO error propag­ation by PCR
Clusters
DNA Nano Balls (DNB)
Polonies

Flowcell

Illumina
MGI
Element Bio
Non Patterned FC
X
Non Patterned FC
Patterned FC
Patterned FC
X
up to 600 cycles (MiSeq)
up to 600 cycles
up to 600 cycles
4 lanes (NovaSeq S4)
4 lanes
2 lanes
up to 12B reads (NovaSeq S4)
1500M-1800M reads
250M-500M-1B reads

Sequencing

Illumina
MGI
Element Bio
Sequencing by synthesis
cPAS sequencing
Sequencing by Avidity
Fluorescent Nucleo­tides
Fluorescent Nucleo­tides
Avidite

Quality

Illumina
MGI
Element Bio
Q30
Q35
Q40
Index Hopping (2%)
Index Hopping (negli­gible)
Avidite (negli­gible)
Duplication (+++)
 
Duplication (low)
AT/GC bias
 
low AT/GC bias

Libraries

Illumina
MGI
Element Bio
   
robust to low diversity libraries
insert size (200–800 bp)
insert size (300-500 bp)
insert size (175-1000 bp)

Illumina platforms

iSeq
MiSeq
NextSeq 2000
NovaSeq 6000
 

MGI platform

DNBSEQ-G400
 

Element Bio platform

AVITI