Cheatography
https://cheatography.com
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 |
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