Labshake search
Citations for Illumina :
101 - 150 of 189 citations for Hrms Rapid Pcb Screening Calibration Solution Cs0.05 Unlabeled 13C12 99% since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Genomics 2022Quote: Genome-wide SNP data from the Illumina Infinium Global Screening Array-24 v1.0 Beadchip (GSA array; Illumina, California, USA) was available for MMNP ...
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bioRxiv - Neuroscience 2024Quote: We measured the genotype of SNP across the genome using the Infinium Global Screening Array-24 v3.0 Kit (Illumina) with the same extracted DNA samples used for the DNA methylation measurement ...
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bioRxiv - Cancer Biology 2024Quote: ... The isolated DNA samples were sent to the Center for Applied Genomics at the Children’s Hospital of Philadelphia for the SNP array analysis using the Infinium Global Screening Array-24 v3.0 Kit (Illumina), which enabled the sequencing of 759,993 SNPs across the genome ...
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bioRxiv - Genomics 2022Quote: ... pooled and sequenced using 12 pM for the loading on rapid flow cells using the HiSeq 2500 system (Illumina). Sequencing mode was set as 20 dark cycles followed by 80 bases in single end reads (SR80).
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bioRxiv - Zoology 2020Quote: ... The library was loaded into a flow cell for cluster generation with the TruSeq Rapid SR Cluster Kit (Illumina) and was sequenced using the Illumina Hiseq 2500 System to obtain single-end 100-nucleotide sequences.
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bioRxiv - Developmental Biology 2022Quote: ... followed by paired end 101 sequencing with single index using the rapid v2 chemistry according to manufacturer’s instructions (Illumina) to a depth of approximately 30M clusters per sample.
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bioRxiv - Genetics 2022Quote: ... Common bi-allelic SNP genotyping was performed using Illumina Global Screening Array SNP-microarray technology (Illumina, San Diego, California, USA). Genotype assignment from the microarray fluorescence data was performed using Illumina’s Genome Studio software.
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bioRxiv - Genetics 2021Quote: WGS of constitutional DNA was performed using the Illumina HiSeq platform as described previously.1 Targeted MBD4 mutation screening was performed (i) using a custom MIP capture panel and sequenced on a NextSeq500 (Illumina) system ...
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bioRxiv - Neuroscience 2023Quote: ... DNA samples for available twin participants were genotyped using the Infinium Global Screening Array-24 v3.0 BeadChip (Illumina, California, USA). Genotyping data is expected to be available in 2023 ...
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bioRxiv - Genomics 2024Quote: ... Total of 778,783 single nucleotide polymorphisms (SNPs) were genotyped on Infinium Global Screening Array MG v3.0 (Illumina, San Diego, CA) by the local service provider (Macrogen ...
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bioRxiv - Genomics 2020Quote: ... Sequencing was carried out on an Illumina Hiseq 2500 using the HiSeq Rapid v2 SBS reagents (Illumina, Little Chesterford, UK), for 150 cycle paired end reads ...
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bioRxiv - Systems Biology 2019Quote: ... The libraries were hybridized to the flow-cell using TruSeq Rapid Duo cBot Sample Loading Kit (Illumina, CT-403-2001), utilising the Illumina RR_TemplateHyb_FirstExt_VR method on the Illumina cBot ...
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bioRxiv - Cancer Biology 2020Quote: ... Single end reads at 50bp were generated by using Hiseq rapid SR cluster kit V2 (Illumina, Cat# GD-402-4002) and HiSeq rapid SBS kit v2 50 cycles (Illumina ...
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bioRxiv - Microbiology 2020Quote: ... 4-5 subsamples per replicate were pooled in equimolar concentrations and sequenced on a HiSeq2500 in a 1×50 bp Rapid Run (Illumina). As the first sequencing run did not deliver sufficient data for seven metatranscriptomes ...
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bioRxiv - Microbiology 2021Quote: ... Sequencing was performed by employing an Illumina HiSeq 2500 system and the HiSeq Rapid SBS kit V2 (2×250 bp) as recommended by the manufacturer (Illumina). Metagenomic reads were further processed as described previously (Eze et al ...
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bioRxiv - Neuroscience 2021Quote: ... Library concentration was determined with an Agilent 2100 Bioanalyzer after which 8 samples were pooled and sequenced using HiSeq Rapid SBS Kit v2 (50 cycles) using paired end reads on a HiSeq2500 (Illumina).
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bioRxiv - Cancer Biology 2021Quote: ... or 150bp/150bp paired end run using the HiSeq Rapid SBS Kit v2 or NovaSeq 6000 SP/S1/S2/S4 Reagent Kit (100/200/300 cycles) (Illumina).
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bioRxiv - Cancer Biology 2020Quote: DNA libraries were generated from 50ng of genomic DNA using the Nextera Rapid Capture Exome kit (Illumina, San Diego, USA) as per manufacturer’s instructions ...
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bioRxiv - Cancer Biology 2020Quote: Sequencing was performed by the Human & Environmental Genomics core facility of Rennes on a HiSeq 1500 (Rapid SBS kit v2 1×100 cycles, Illumina). Base Calling was performed with Illumina’s CASAVA pipeline (Version 1.8).
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bioRxiv - Genomics 2019Quote: ... The sequencing library with the mean insert size of 429bp (agarose gel, fraction E) was sequenced using TruSeq Rapid SBS Kit v2 (Illumina), in paired end mode ...
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bioRxiv - Neuroscience 2021Quote: ... Sequencing was carried out by running 150 cycles on Illumina HiSeq 2500 using TruSeq Rapid SBS Kit (FC-402-4001, Illumina) according to the manufacturer’s instructions.
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bioRxiv - Immunology 2021Quote: ... Libraries were sequenced on a NovaSeq 6000 Illumina platform to obtain 50-bp paired end reads (TruSeq Rapid kit; Illumina).
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bioRxiv - Microbiology 2023Quote: ... the library was denatured with 0.1 M NaOH to generate single-stranded DNA molecules and loaded into flow cell channels at a concentration of 8 pM and amplified in situ using TruSeq Rapid SR cluster kit (# GD-402-4001, Illumina). Sequencing was performed at 100 cycles on the Illumina HiSeq 4000 according to the manufacturer’s instructions.
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bioRxiv - Molecular Biology 2022Quote: ... and high-throughput sequencing was performed on an Illumina HiSeq 2500 sequencer with a HiSeq Rapid v2 Reagent Kit (Illumina). The sequences of 2 × 250 bp paired-end reads were produced from the sequencer following the manufacturer’s instructions ...
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bioRxiv - Plant Biology 2023Quote: Sequencing of libraries was carried out on a HiSeq2500 sequencing platform using HiSeq Rapid SR Cluster Kit v2 (Illumina, USA) and HiSeq Rapid SBS Kit v2 (50 Cycle ...
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bioRxiv - Cancer Biology 2023Quote: ... and sequenced as 100 base single end reads on an Illumina HiSeq 2500 using TruSeq Rapid SBS sequencing kit version 1 and HCS version 2.0.12.0 data collection software (Illumina, San Diego, CA). Base-calling is performed using Illumina’s RTA version 1.17.21.3 ...
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bioRxiv - Cancer Biology 2023Quote: ... The libraries were run in the rapid run flow cell and were single end sequenced (65 bp) on HiSeq 1500 (Illumina).
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bioRxiv - Genomics 2024Quote: ... The samples had been sequenced using either the Illumina HiSeq 2500 platform using the HiSeq Rapid SBS Kit v2 500-cycles (Illumina) or the MiSeq platform (Illumina ...
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bioRxiv - Plant Biology 2024Quote: ... NEXTflexTM Rapid DNA-seq Library Prep Kit was used to prepare and index libraries before sequencing on HiSeq 2500 (Illumina) with two lanes per sample ...
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bioRxiv - Genomics 2020Quote: ... a total of 936 DNA samples were sent for genome-wide SNP genotyping using the Infinium Global Screening Array (GSA) with Shared Custom Content (Illumina Inc.). After extensive QC and imputation ...
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bioRxiv - Neuroscience 2019Quote: Buccal swab and saliva samples were collected for DNA extraction followed by genome-wide genotyping using the “Global Screening Array” (Illumina, Inc). For a full description of genotyping and post-genotyping methods ...
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bioRxiv - Genetics 2022Quote: ... Genotyping was performed with the Illumina Infinium Global Screening Array 1.0 with MDD and Psych content (Illumina, San Diego, CA, USA) at the Life & Brain facilities (Bonn ...
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bioRxiv - Genomics 2019Quote: ... resulted in 936 DNA samples of sufficient quality and quantity to attempt genome-wide SNP genotyping using the Infinium Global Screening Array (GSA) with Shared Custom Content (Illumina Inc.). GSA genotyping was performed at the Institute of Clinical and Medical Biology (UKSH ...
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bioRxiv - Genomics 2021Quote: ... Genome-wide SNP genotyping data were generated from the same samples using the “Global Screening Array” (GSA) with shared custom content (Illumina, Inc.) using procedures outlined in Hong et al ...
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bioRxiv - Neuroscience 2023Quote: ... and the University of California Los Angeles) on three genotyping platforms (Illumina Human660W, Illumina OmniExpress 2.5, and Illumina Global Screening Array) in 10 total batches (Supplementary Figure 1) ...
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bioRxiv - Microbiology 2019Quote: ... A paired-end 150-bp sequencing run was performed using the Illumina Rapid Run on an Illumina HiSeq 2500 platform (Illumina, Denmark), according to manufacturer’s instructions.
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bioRxiv - Genetics 2020Quote: ... we used the NEXTFLEX® Rapid DNA-Seq Kit 2.0 for Illumina paired-end sequencing library (Illumina, San Diego, CA, USA) and the xGen hybridization capture system with Exome Research Panel v2 (Integrated DNA Technologies ...
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bioRxiv - Evolutionary Biology 2022Quote: ... in the DNA Sequencing Section at the Okinawa Institute of Science and Technology Graduate University using HiSeq Rapid SBS Kit v2 kit (500 cycles, Illumina, USA) yielding 250-bp paired-end reads (Fig ...
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Age, sex, and cell type-resolved hypothalamic gene expression across the pubertal transition in micebioRxiv - Genomics 2023Quote: ... Single-read 50-bp sequencing was performed at TCAG on an Illumina HiSeq2500 Rapid Run or V4 flowcell (Illumina, San Diego) with cycles extended to 68 bp.
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bioRxiv - Cancer Biology 2023Quote: DNA libraries were produced from 50 ng of genomic DNA using the Nextera Rapid Capture Exome kit (Illumina, San Diego, USA) as per manufacturer’s instructions ...
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bioRxiv - Neuroscience 2021Quote: ... Genotyping was performed using single nucleotide polymorphism (SNP) microarrays (Infinium Global Screening Array v2.4. or Infinium OmniExpress-24; Illumina, San Diego, CA). Raw genotype files were converted to PLINK-compatible files using GenomeStudio software (Illumina ...
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bioRxiv - Pathology 2021Quote: Genotyping was performed using single nucleotide polymorphism (SNP) microarrays (Infinium Global Screening Array v2.4. or the Infinium OmniExpress-24, Illumina, San Diego CA). Raw genotype files were converted to PLINK-compatible files using GenomeStudio software (Illumina ...
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bioRxiv - Genetics 2021Quote: ... Genotyping was carried out using the Illumina Infinium Global Screening Array 1.0 with MDD and Psych content (Illumina, San Diego, CA, USA) at the Life & Brain facilities ...
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bioRxiv - Genomics 2019Quote: ... Genotyping for the discovery cohort was performed using the Illumina Global Screening Array-24 v1.0 BeadChip (Illumina, Inc., San Diego, CA, USA). Quality control for the SNP and individuals are described in the supplemental methods ...
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bioRxiv - Genetics 2023Quote: ... additional OGM findings were confirmed with the SOC methods karyotyping and the Infinium Global Screening Array-24 v3.0-EA-MD (SNP-Array) (Illumina, San Diego, CA), according to standard protocols ...
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The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental developmentbioRxiv - Genetics 2024Quote: ... The Illumina Global Screening Array platform was used (v3.0) (Infinium HTS Assay Reference Guide (# 15045738 v04) (Illumina, Inc. San Diego, CA, USA). Output data were analyzed in Illumina Genome Studio version 2.0 ...
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bioRxiv - Evolutionary Biology 2024Quote: ... which were the Infinium Global Screening Array-24 Kit™ (GSA24) and the Infinium Global Diversity Array-8 Kit™ (GDA8) from Illumina and the Axiom™ Genome-Wide Human Origins (HO ...
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bioRxiv - Plant Biology 2020Quote: ... The library pool was sequenced 2x 70 nt paired-end using rapid run mode on Illuminàs HiSeq 1500 50% (Illumina, San Diego, California). Paired end reads of triplicated Wt and hit1 samples were mapped onto the transcriptome v5.5 of Chlamydomonas reinhardtii with kallisto (Bray et al. ...
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bioRxiv - Cancer Biology 2020Quote: ... Sequencing was performed at The Centre for Applied Genomics (Toronto, Canada) across 2 lanes of an Illumina HiSeq2500 rapid run flowcell (Illumina, San Diego) with SR100 bp.
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bioRxiv - Cancer Biology 2019Quote: ... 50ng of gDNA was used as the input and the sequencing libraries were prepared using the Illumina® Nextera Rapid Capture Enrichment kit (Illumina Inc.). The steps included tagmentation of gDNA ...