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Pe 102 1003

Manufactured by Qiagen

The PE‐102-1003 is a laboratory equipment product manufactured by Qiagen. It is designed to perform a core function within the laboratory setting. No further details about its intended use or capabilities can be provided in an unbiased and factual manner.

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2 protocols using pe 102 1003

1

Illumina Sequencing Library Preparation

Check if the same lab product or an alternative is used in the 5 most similar protocols
DNA was extracted using the Qiagen DNeasy Blood and Tissue Kit and sheared using a Covaris E220 (Woburn, MA) (duty cycle 10, intensity 5, cycles/burst 200 and time 180 s) to ~400 base pair (bp). Sheared genomic DNA was gel purified and used as input for Illumina sequencing library prep, with end-repair using the NEBNext end-repair kit (E6050L), and A-tailing with Taq polymerase. Ligation to Illumina paired-end adapters (PE‐102-1003) was done using Ultrapure ligase (L603-HC-L) from Enzymatics, and amplification with iProof (Bio-Rad). Agencourt Ampure XP beads were used for clean-up and size selection at each step. The resulting DNA library was sequenced on a single lane of an Illumina HiSeq2000 at the Stanford Center for Genomics and Personalized Medicine.
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2

DNA Extraction, Shearing, and Library Prep

Check if the same lab product or an alternative is used in the 5 most similar protocols
DNA was extracted using the Qiagen DNeasy Blood and Tissue Kit and sheared using a Covaris E220 (Woburn, MA) (duty cycle 10, intensity 5, cycles/burst 200, time 180 sec) to approximately 400 base pair (bp). Sheared genomic DNA was gel purified and used as input for Illumina sequencing library prep, with end-repair with NEBNext end-repair kit (E6050L), and A-tailing with Taq polymerase. Ligation to Illumina paired-end adapters (PE-102-1003) was done using Ultrapure ligase (L603-HC-L) from Enzymatics, and amplification with iProof (BioRad). Agencourt Ampure XP beads were used for clean-up and size selection at each step. The resulting DNA library was sequenced on a single lane of an Illumina HiSeq2000 at the Stanford Center for Genomics and Personalized Medicine.
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