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Single Cell Sequencing Service For Cancer

The document discusses next-generation sequencing service and principles. It describes the key steps in NGS which are DNA library preparation, clonal amplification to form DNA clusters, and cyclic array sequencing to obtain fragment sequences which are then assembled into contigs.

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Shaw Vivian
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0% found this document useful (0 votes)
48 views1 page

Single Cell Sequencing Service For Cancer

The document discusses next-generation sequencing service and principles. It describes the key steps in NGS which are DNA library preparation, clonal amplification to form DNA clusters, and cyclic array sequencing to obtain fragment sequences which are then assembled into contigs.

Uploaded by

Shaw Vivian
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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NEXT GENERATION

SEQUENCING SERVICE
Next-generation sequencing 1 DNA Library Preparation 2 Clonal Amplification
(NGS) technologies have
progressive advantages in 1 2 3
terms of cost-effectiveness,
unprecedented sequencing
speed, high resolution and
accuracy in genomic analy-  
ses, thus are playing an
increasing important role in 4 5
fields of oncology and immu-
nology.

The sequencing principles of


common sequencing instru- 
ments on the market: (1) first, 
construct a DNA template
library. Obtain DNA library
fragments (tens to hundreds
of bases in length) by
randomly breaking genomic
DNA, or construct paired-end
fragments that control the
distance distribution. Adapter
sequences were ligated to
both ends of the DNA 
fragment and then denatured   
to obtain a single-stranded
template library and immobi-
lized on a solid surface. (2) 3 Cyclic Array Sequencing
Second, amplify the clones,
which performed by one of 
  
  
several methods, such as
3'
5'
3'
5'

3'
5'

3'
5'


3'
5'
bridge PCR and emulsion 
 
PCR. (3) Then, forming DNA T   

A
clusters or amplifying micro-
A

A
A
T
A
T

A
T

A
A
 
spheres of DNA cluster arrays C
A
 
on a chip, performing a series A
A

 
A
A


of cyclic reaction operations  
using a polymerase\ or ligase, 
 
and monitoring the optical 
    
events generated in each
cycle biochemical reaction by
a microscopic detection syst-
 
 

em. Time series analysis of 3' GA CAn n n z z
 
the resulting array images is  zz
z
A C G T nn 3'
performed to obtain sequenc- GA n CT GT
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es of DNA fragments. These
fragments are then assem- C 3'


3' GA CA
CT
bled into longer contigs G  
   3'
CT GT
according to certain computer T


algorithms.
z GA CA TA AA
z z
GA n n n
3' 5' 3' 5' 3' 5'
Creative Biolabs uses the AAn n n z z z CAn n n z z z CT GT AT TT
advanced SuPrecision™ pl- 3' 
CT
3' 5' 3' 5'  T G CC GT
atform to support researchers GA n n n z z z TAnnn z z z
all over the world with their

   AC GG CA
sequencing needs for cancer. 

WHAT WE DO:
Whole Genome Sequencing (WGS)
Creative Biolabs Service for Cancer
Whole Transcriptome Sequencing (WTS)
Service for Cancer
Next Generation Whole Exome Sequencing (WES) Immune Repertoire Sequencing (Rep-seq)
Service for Cancer
Sequencing Service for Cancer
Targeted Sequencing Service for Bioinformatics Analysis Service
Service Cancer

© 2007 - 2019 Creative-Biolabs All Rights Reserved Email: info@creative-biolabs.com Tel: 1-631-381-2994

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