From 6113331d48b5e8a578d8eba832b0115aa0681f1b Mon Sep 17 00:00:00 2001 From: Sabrina Zander <sabrina.zander@uni-duesseldorf.de> Date: Tue, 21 Jan 2025 11:25:29 +0100 Subject: [PATCH] add assay 2_1 --- .gitattributes | 8 ++++++++ assays/2-1_Sequencing and Analysis/README.md | 0 .../dataset/.gitkeep | 0 .../RawReads/Background/His-Background.7z | 3 +++ .../RawReads/Background/Strep-Background.7z | 3 +++ .../dataset/RawReads/Heme/DtxR_heme.7z | 3 +++ .../dataset/RawReads/Heme/HrrA_heme.7z | 3 +++ .../dataset/RawReads/Iron/DtxR_Iron.7z | 3 +++ .../dataset/RawReads/Iron/HrrA_Iron.7z | 3 +++ .../RawReads/Starvation/DtxR_Starvation.7z | 3 +++ .../RawReads/Starvation/HrrA_Starvation.7z | 3 +++ .../2-1_Sequencing and Analysis/isa.assay.xlsx | Bin 0 -> 12426 bytes .../protocols/.gitkeep | 0 .../protocols/Sequencing.txt | 1 + 14 files changed, 33 insertions(+) create mode 100644 assays/2-1_Sequencing and Analysis/README.md create mode 100644 assays/2-1_Sequencing and Analysis/dataset/.gitkeep 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b/assays/2-1_Sequencing and Analysis/protocols/Sequencing.txt @@ -0,0 +1 @@ +The isolated DNA fragments were used for library preparation and indexing with TruSeq DNA PCR-free sample preparation kit (Illumina, Chesterford, UK) according to manufacturer’s instructions, leaving out the DNA size selection steps. Libraries were quantified using KAPA library quant kit (Peqlab, Bonn, Germany) and normalized for pooling. These pooled libraries were sequenced using the MiSeq device (Illumina) (paired-end sequencing, read length: 2 x 150 bases). \ No newline at end of file -- GitLab