Format

Send to:

Choose Destination

SRX327895: De-novo transcriptome analysis of intestinal fluke Fasciolopsis buski
1 ILLUMINA (Illumina Genome Analyzer II) run: 42.4M spots, 7.6G bases, 4.1Gb downloads

Design: •2 ug micrograms of genomic DNA for each sample was made up to 100 ul with nuclease free water (Ambion) and sonicated using a Bioruptor (Diagenode) to obtain desired fragment length ranging between 150 to 600 bp for short insert library and 200 to 600 bp for long insert library. •Fragmentation conditions (Bioruptor) •FD2 Short insert library – (30 pulses at high for 30s ON and 30s OFF). Sonication was repeated with the same conditions for another aliquot of 2 ug. •FD2 Long insert library – (20 pulses at high for 30s ON and 30s OFF) •The size distribution was checked by running an aliquot of the sample on Agilent 7500 Bioanalyzer Chip. The fragmented DNA was cleaned up using 0.7X Agencourt Ampure XP SPRI beads (Beckman Coulter) for long insert libraries and 1.8X Agencourt for short insert libraries. Yield of Recovered DNA after fragmentation FD2 Short insert library: – (464 ng for 1st aliquot, 1472 ng for 2nd aliquot). The recovered DNA from both aliquots were pooled and 1 ug was taken for library preparation FD2 Long insert library: – (1281 ng). 1 ug was taken for library preparation Subsequently libraries for whole genome sequencing were constructed according to the TruSeq DNA library protocol outlined in “TruSeq DNA Sample preparation guide”. DNA was subjected to a series of enzymatic reactions that repair frayed ends, phosphorylate the fragments, and add a single nucleotide ‘A’ overhang and ligate adaptors (Illumina’s TruSeq DNA sample preparation kit). Sample cleanup was done using Ampure XP SPRI beads. After ligation, ~300-350 bp fragment for short insert libraries and ~500 – 550 bp fragment for long insert libraries was size selected by gel electrophoresis, gel extracted and purified using Minelute columns (QIAGEN). The libraries were amplified using 10 cycles of PCR for enrichment of adapter-ligated fragments. The prepared libraries were quantified using Nanodrop and validated for quality by running an aliquot on High Sensitivity Bioanalyzer Chip (Agilent).
Submitted by: NEHU
Study: Fasciolopsis buski Transcriptome or Gene expression
show Abstracthide Abstract
Fasciolopsis buski is a socioeconomically important and one of the largest intestinal flukes of pigs and humans with a flat and thick body of 2-10 cm in length and 0.8-3 cm in width that causes the disease fasciolopsiasis. The infective cysted stages of this flatworm develop on the surface of aquatic plants, eg. Water caltrop and reach their host due to ingestion of such contaminated vegetation. In several countries, this neglected tropical disease is aggravated by factors, such as poverty, malnutrition, and an uncontrolled food market associated with lack of food inspection, poor sanitation, and other helminthiases. Although fasciolopsiasis can be controlled along with other food-borne parasitoses, it still remains a public health problem in many endemic areas including India despite sustained WHO control programmes. The parasite is a close relative of liver flukes (Fasciola). Very little is known about this parasite and its relationship with its hosts at the molecular level. Here, we carried out advanced sequencing and bioinformatic technologies employed to explore the genes transcribed in the adult stage of F. buski.
Sample: Clinical or host-associated pathogen sample for Fasciolopsis buski
SAMN02221882 • SRS454042 • All experiments • All runs
Library:
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: DNase
Layout: PAIRED
Spot descriptor:
forward101  reverse

Runs: 1 run, 42.4M spots, 7.6G bases, 4.1Gb
Run# of Spots# of BasesSizePublished
SRR94313942,425,9887.6G4.1Gb2015-07-22

ID:
456840

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center