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Citations for Illumina :
651 - 700 of 790 citations for T Cell Surface Glycoprotein CD3 Gamma Chain CD3G Antibody Biotin since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Molecular Biology 2024Quote: ... and clustered on an Illumina Novaseq 6000 S4 flow cell followed by 150bp paired-end sequencing with inclusion of 10-15% spike-in PhiX Control v3 library (Illumina). Controlled access to DNase-seq ...
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bioRxiv - Genetics 2023Quote: ... Samples were sequenced using 75 bp paired-end sequencing (reverse stranded) on a NovaSeq 6000 system (S4 flow cell, Xp workflow; Illumina).
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bioRxiv - Developmental Biology 2023Quote: ... and then 50 nucleotide paired-end DNA sequencing was completed on an Illumina NovaSeq 6000 system using a S1 flow cell (Illumina). Raw RNAseq reads are available at the SRA under accession (Not uploaded yet).
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bioRxiv - Developmental Biology 2023Quote: ... cells (sample of all leg disc cells) from three different replicates were sent to Heidelberg genomic platform EMBL for high-throughput mRNA sequencing (NextSeq 500/Illumina). They generated mRNA libraries with NEB RNA Ultra kit (New England Biolabs E7770L ...
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bioRxiv - Developmental Biology 2023Quote: ... Barcoded cDNA libraries were multiplexed onto a TruSeq paired-end flow cell and sequenced (100-bp paired-end reads) with a TruSeq 200-cycle SBS kit (Illumina). Samples were run on an Illumina NovaSeq 6000 sequencer at the KUMC Genome Sequencing Facility ...
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bioRxiv - Immunology 2023Quote: ... Single-cell RNA libraries were prepared according to the 10x Genomics Chromium Single Cell 3′ Reagent Kits v2 User Guide and sequenced (paired-end) on a HiSeq 4000 (Illumina).
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bioRxiv - Pathology 2024Quote: ... The cDNA libraries were prepared using a Chromium Single Cell 3’ V3 kit (10X Genomics, USA) according to the manufacturer’s instructions and then sequenced on a NovaSeq6000 (Illumina, USA). Raw sequencing reads were aligned to the mm10 (GENCODE vM23/Ensembl 98 ...
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bioRxiv - Cancer Biology 2024Quote: ... This multiplexed pool was sequenced with the following parameters with an S2 flow cell on the NovaSeq 6000 platform (Illumina): Read 1 – 28 cycles ...
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bioRxiv - Cancer Biology 2024Quote: ... library preparation was performed using a modified single-cell whole-genome sequencing protocol and 77 base pair single reads were generated using a NextSeq 500 sequencing instrument (Illumina). From each assessed case ...
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bioRxiv - Genomics 2024Quote: ... 4.5 µl of sample were used to generate single cell RNA-Seq libraries by following the Illumina Bio-Rad SureCell WTA 3’ Library Prep Guide (Illumina, San Diego CA and Bio-Rad ...
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bioRxiv - Immunology 2024Quote: ... After centrifugation at 500ξ g for 5min at 4°C, the cell pellets were resuspended in tagmentation-mix (containing Tagment DNA buffer, Tagment DNA Enzyme (Illumina), Digitonin (Promega ...
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bioRxiv - Developmental Biology 2024Quote: ... Barcoded cDNA libraries were multiplexed onto a TruSeq paired-end flow cell and sequenced (100-bp paired-end reads) with a TruSeq 200-cycle SBS kit (Illumina). Samples were run on Illumina HiSeq2500 sequencers located at the KUMC Genome Sequencing Facility ...
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bioRxiv - Cancer Biology 2024Quote: ... RNA-seq libraries for the cell lines and the CLL RNA were prepared using the TruSeq-stranded-total RNA SamplePrep kit (Illumina) according to the manufacturer’s protocol ...
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bioRxiv - Cancer Biology 2021Quote: ... The INA-6 cells were sequenced (18 million reads per sample) using the TruSeq Stranded mRNA library preparation kit from Illumina (#20020595) followed by 75bp single read sequencing on the Illumina Hiseq 4000 next machine ...
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bioRxiv - Immunology 2021Quote: ... The amplified libraries were hybridized to the Illumina flow cell and sequenced using the NextSeq 550 sequencer (Illumina, San Diego, CA). Single end reads of 75nt were generated for each sample ...
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bioRxiv - Neuroscience 2020Quote: ... Sequencing libraries (1.3 nM) were chemically denatured and applied to an Illumina NovaSeq flow cell using the NovaSeq XP chemistry workflow (Illumina-20021664). Following transfer of the flowcell to an Illumina NovaSeq instrument ...
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bioRxiv - Evolutionary Biology 2021Quote: ... libraries were sequenced using 100 base-length read chemistry in paired-end flow cell on the Illumina HiSeq2000 (Illumina®, USA).
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bioRxiv - Neuroscience 2020Quote: ... The cell solutions were immediately transferred to ice and transported to the Wellcome Trust Centre for Human Genetics (WTCHG) for scRNAseq via 10x genomics chromium (10x genomics, US) (Single Cell 3’ v3) and Illumina hiseq 4000 (Illumina, US). This approach achieved 66-72K mean reads per cell and a sequencing depth of 53-55% per cell before filtering.
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bioRxiv - Genomics 2020Quote: ... CNV analysis was performed on a combined cohort of 130 sequenced hESC lines and a control cohort consisting of 243 human samples from primary blood or lymphoblastoid cell lines (LCL) that had undergone WGS on the same platform (Illumina HiSeqX) and to similar depth as the hESC lines (Pato et al. ...
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bioRxiv - Cell Biology 2022Quote: ... Diluted libraries were multiplex-sequenced and run on a HiSeq 2000 Illumina platform in HiSeq Flow Cell v3 (Illumina Inc., USA) using TruSeq SBS Kit v3 (Illumina Inc. ...
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bioRxiv - Neuroscience 2021Quote: ... The amplified libraries were hybridized to the Illumina single end flow cell and amplified using the cBot (Illumina, San Diego, CA) at a concentration of 8 pM per lane ...
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bioRxiv - Genomics 2020Quote: ... The amplified libraries were hybridized to the Illumina single end flow cell and amplified using the cBot (Illumina, San Diego, CA). Single end reads of 100nt were generated for each sample using Illumina’s HiSeq2500v4.
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bioRxiv - Genomics 2020Quote: ... The amplified libraries were hybridized to the Illumina single end flow cell and amplified using the cBot (Illumina, San Diego, CA). Single end reads of 100nt were generated for each sample using Illumina’s HiSeq2500v4.
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bioRxiv - Molecular Biology 2021Quote: ... Libraries from knockout FL83B cells and their corresponding non-targeting controls were prepared with TruSeq Stranded mRNA Library Kit (Illumina, #20020595), pair-end sequencing was performed using the NovaSeq 6000 (Illumina) ...
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bioRxiv - Molecular Biology 2021Quote: Libraries from human liver tissue and wild type FL83B cells were prepared with TruSeq Stranded Total RNA Library Prep Gold (Illumina, #20020599), single-read sequencing was performed using the NextSeq 500 (Illumina) ...
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bioRxiv - Cancer Biology 2020Quote: ... The amplified libraries were hybridized to the Illumina single end flow cell and amplified using the cBot (Illumina, San Diego, CA). Single end reads of 75nt were generated for each sample using Illumina’s NextSeq55036.
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bioRxiv - Plant Biology 2020Quote: ... sequencing was performed with the Illumina NovaSeq 6000 system using S1 flow cell with lane divider (Illumina, San Diego, CA, USA). Read length for the paired-end run was 2 x 101 bp ...
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bioRxiv - Cancer Biology 2020Quote: ... and 2000 copies/cell yeast SUMO to each sample then proceed with rRNA removal Ribo Zero Gold kit (Illumina cat # MRZ11124C) according to manufacturer’s protocol ...
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bioRxiv - Cancer Biology 2022Quote: ... but from purified CLL cells (Miltenyi B-CLL Isolation kit) and sequenced on an Illumina HiSeq 4000 (Illumina, Hayward, CA, USA). miRNA data in the form of fastq were quality checked using FastQC ...
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bioRxiv - Microbiology 2020Quote: ... Short reads were obtained using NovaSeq6000 S2 Reagent Kit (300cycles) and S2 flow cell on a NovaSeq6000 (2×150-bp paired-end) system (Illumina, USA) at Eurofins Genomics GmbH ...
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bioRxiv - Zoology 2021Quote: ... We shipped the unfrozen DNA with freezer packs to the University of Oregon’s Genomics and Cell Characterization Core Facility (https://gc3f.uoregon.edu/) for 150bp single-end sequencing on an Illumina HiSeq 4000 (Illumina, San Diego, CA).
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bioRxiv - Developmental Biology 2019Quote: Single cell 3’ RNA-seq experiments were conducted using the Chromium single cell system (10x Genomics, Inc) and the NexSeq 500 sequencer (Illumina, Inc). Approximately 10,000 cells per sample were added to a single cell master mix ...
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bioRxiv - Synthetic Biology 2019Quote: ... The RNAseq data was generated on an Illumina NextSeq500 75 SE high-output flow-cell (Illumina, cat no. FC-404-2005). The run yielded approximately 550 million reads ...
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bioRxiv - Molecular Biology 2020Quote: The OmniATAC transposition reaction was performed with 50000 mES cells as previously described (Corces et al., 2017) using the Tagment DNA TDE1 Enzyme (Illumina, #20034197). DNA was purified using the PCR clean-up MinElute kit (Qiagen ...
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bioRxiv - Genomics 2021Quote: ... Each library was sequenced using 100 base-length read chemistry on a paired-end flow cell on the Illumina HiSeq2000 (Illumina, USA).
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bioRxiv - Genomics 2021Quote: ... The libraries were sequenced using 251 base- length read chemistry in a paired-end flow cell on the Illumina HiSeq2500 sequencer (Illumina, USA).
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Altered TGFB1 regulated pathways promote accelerated tendon healing in the superhealer MRL/MpJ mousebioRxiv - Cell Biology 2021Quote: ... The amplified libraries were hybridized to the Illumina single end flow cell and amplified using the cBot (Illumina, San Diego, CA). Single end reads of 100nt were generated for each sample ...
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bioRxiv - Genetics 2019Quote: ... Equimolar amounts of each library were loaded on a Next-Seq Mid output flow cell cartridge (Illumina NextSeq 500/550 #20022409).
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bioRxiv - Neuroscience 2022Quote: ... We pooled up to 12 samples (with different barcodes) in one lane of a flow cell for sequencing (Illumina HiSeq 2500) and used a 150 bp paired-end read configuration ...
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bioRxiv - Developmental Biology 2022Quote: ... Then the cells were precipitated and kept on ice and subsequently resuspended in 25μl 2X Tagment DNA Buffer (Illumina Nextera kit), 2.5μl Transposase enzyme (Illumina Nextera kit ...
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bioRxiv - Systems Biology 2023Quote: ... centrifuged at 350g for 5 minutes and resuspended and put through a Flowmi™ strainer (before cell counts were carried out for sample preparation, see 10x Illumina Single Cell Library Preparation and RNA Sequencing).
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bioRxiv - Genomics 2022Quote: ... Each library was sequenced using 151 base-length read chemistry on a paired-end flow cell on the Illumina HiSeq4000 sequencing platform (Illumina, USA).
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bioRxiv - Molecular Biology 2023Quote: ... 1 x 105 mESCs and 5 x 104 S2 cells were resuspended in Tagment DNA Buffer and treated with 3 µL TDE1 Tagment DNA Enzyme (Illumina 20034197). After thorough mixing ...
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bioRxiv - Molecular Biology 2023Quote: ... A 1.4 nM pool of each QC passed RNA-seq library was sequenced by running a Single Read (SR) 100bp NovaSeq 6000 S2 flow cell on the NovaSeq 6000 Sequencing System (Illumina, Inc.). The fastq files were obtained by demultiplexing the bcl basecall files using the 1.8.4 version bcl2fastq script (Illumina ...
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bioRxiv - Cell Biology 2024Quote: ... libraries were sequenced on a High-output flow cell (400M clusters) using the NextSeq® 500/550 High Output 150 cycles kit (Illumina), in paired- end 76/76 nt mode ...
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bioRxiv - Genomics 2023Quote: ... The pool was sequenced on an entire lane of a NextSeq 500 HO flow cell to generate paired-end 151 bp reads using the NextSeq 500 High Output Kit v2.5 (300 cycles) (Illumina, Cat # 20024908).
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bioRxiv - Microbiology 2023Quote: ... transcriptomic libraries were generated and sequenced on an Illumina NovaSeq 6000 (S4 flow cell, 100bp paired-end; Illumina, San Diego, CA). Raw data is available in the NCBI SRA under the accession number PRJNA857920 ...
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bioRxiv - Genomics 2023Quote: 1 ng of psoralen pull-down DNA (or corresponding Input DNA from the same cells without pull-down) was used to prepare sequencing libraries using a Nextera XT library prep kit (Illumina, Inc) according to the manufacturer protocol ...
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bioRxiv - Genomics 2023Quote: ... Each library was sequenced using 151 base-length read chemistry on a paired-end flow cell on the Illumina NovaSeq6000 (Illumina, USA). After Illumina sequencing ...
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bioRxiv - Neuroscience 2024Quote: ... Sequencing of the 10x Genomics single-cell RNA-seq libraries was performed on an Illumina NovaSeq 6000 (Illumina, San Diego, CA) at the sequencing core facility of the Max Planck Institute for Molecular Genetics (Berlin ...