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Normalized and Subtracted cDNA Libraries


Normalized libraries .

One way to avoid the repetitive and expensive sequencing of highly redundant cDNAs is to use a normalized library. Normalization equalizes the representation of all transcripts in the cDNA population (overview of the method). Thus the identification of novel and rare transcripts is enhanced (Table 1).  Additionally, cDNA from different tissue sources can be independently tagged during cDNA synthesis for identification of transcript source after sequencing.

 

Subtracted libraries

During mass sequencing of normalized cDNA libraries in the Keck Center, redundancy is continuously monitored by sequence assembly. When identification of novel transcripts falls below 50%, a molecular subtraction of the already sequenced clones is performed (overview of the method). The resulting subtracted library is enriched for low abundance transcripts that are commonly missed in conventional sequencing (Table 1). The technique is also used to subtract commonly expressed clones from previous libraries.

 

 

Table 1. Data from normalized and subtracted libraries constructed in the Keck Center.

 

Normalized

 

Subtracted

Library

# Sequences

% Unique cDNAs

 

Total # of  Sequences

% Unique cDNAs

Zebra Finch (brain)

18,240

59%

 

35,000

49%

Planarian

5,000

60%

 

16,320

57%

Maize (root)

6,000

65%

 

 

 

Horse (cartilage)

16,319

59%

 

 

 

Corn Rootworm

11,149

48%

 

14,921

50%

Pig (uterus, hypothalamus)

10,000

60%

 

 

 

Cattle (placenta)

5,047

68%

 

12,777

64%

Honey Bee (brain)  

7,968

60%

 

15,311

59%

Cassava

8,956

66%

 

 

 

Cassava drought

9,210

60%

 

 

 

Leafy Spurge

10,226

44%

 

20,928

55.4%

Number of sequenced clones and percentage of cDNAs identified as unique upon assembly in normalized libraries and, in some cases, after subtraction and further sequencing. In both normalized and subtracted libraries the identification of unique sequences is substantially enhanced.

 

Materials provided by the researcher:

-         Tissue (2-10g depending on the source), or

-         High-quality total RNA (1-2mg) 

 

Services performed by the Keck Center:

-      Isolation of total RNA and poly(A) RNA

-        cDNA synthesis and size fractionation from 0.5kb (unless otherwise indicated by the PI)

-        Cloning into pBluescript II or your vector of choice

-        Transformation into E.coli electrocompetent cells

-        Normalization

-      Sequencing of 192 clones. Vector and quality trimmed sequences are assembled to determine sequence  similarity and redundancy and identity is determined by comparison to specific databases.

 

Subtraction is normally performed for libraries constructed and sequenced in the Keck Center. The efficiency of subtraction is determined by sequencing 192 clones as described above.

Custom services will be considered

Pricing

 


High Throughput Sequencing and Genotyping Unit
Shahjahan Ali 1201 W. Gregory Drive, Urbana, IL 61801
Phone: (217) 244-3480     FAX: (217) 265-5066      Email:shahjahan@life.uiuc.edu

Last edited: 1 Nov 2006