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Citations for Illumina :
351 - 400 of 9374 citations for Prostaglandin E2 PGE2 Multi Format ELISA Kit 1 Whole Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Developmental Biology 2023Quote: ... Libraries were quantified using the KAPPA quantification kit following manufacturers protocol after which the plates were sequenced on the NextSeq 500 (Illumina) for 25 million reads per plate.
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bioRxiv - Cancer Biology 2019Quote: ... the Midi plate from Illumina’s Rapid Capture Exome kit was replaced with a skirted PCR plate to facilitate automation ...
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bioRxiv - Cancer Biology 2019Quote: ... the Midi plate from Illumina’s Nextera Exome Kit was replaced with a skirted PCR plate to facilitate automation ...
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bioRxiv - Genetics 2021Quote: Participants in the South African Zulu study were genotyped using the Illumina Multi-Ethnic Genotyping Array (Illumina, Illumina Way, San Diego, CA, USA). The Affymetrix Axiom PANAFR SNP array or Illumina Multi-Ethnic Genotyping Array was used to genotype participants in the AADM study ...
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bioRxiv - Genetics 2021Quote: Participants in the South African Zulu study were genotyped using the Illumina Multi-Ethnic Genotyping Array (Illumina, Illumina Way, San Diego, CA, USA). The Affymetrix Axiom PANAFR SNP array or Illumina Multi-Ethnic Genotyping Array was used to genotype participants in the AADM study ...
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bioRxiv - Genomics 2021Quote: ... We include QCed genotypes generated in the GCAT cohort with the Infinium Expanded Multi-Ethnic Genotyping Array (MEGAEx) (ILLUMINA, San Diego, California, USA) as described elsewhere18 (i.e ...
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bioRxiv - Microbiology 2021Quote: ... according to the manufacturer’s instructions and whole-genome sequencing was performed on an in-house MiSeq platform (Illumina). For long-read sequencing ...
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bioRxiv - Developmental Biology 2020Quote: ... Whole-genome 2X100 bp or 2X150 bp paired-end sequencing was performed on HiSeq_2500 or Novaseq 6000 (Illumina). Supplemental Table S1 provides basic sequencing statistics for all samples used in this study.
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bioRxiv - Microbiology 2020Quote: ... Libraries were subjected to whole-genome sequencing using an Illumina® MiSeq benchtop devise (Illumina, San Diego, CA) in paired-end mode (v3 chemistry ...
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bioRxiv - Genetics 2019Quote: The whole genome genotyping was performed on 80 ovine genomic DNA using the OvineSNP50 Genotyping Beadchip from Illumina according to the manufacturer’s protocol at the Laboratoire d’Analyses Génétiques pour les Espèces Animales ...
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bioRxiv - Plant Biology 2021Quote: ... and the whole transcriptomes were sequenced using the 100 bp paired-end mode on a HiSeq 2500 (Illumina). The raw read files are deposited as PRJNA742033 in NCBI.
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bioRxiv - Microbiology 2021Quote: Whole-genome sequencing (WGS) of 31 EIEC strains used in a previous study (26) was performed by Illumina NextSeq (Illumina ...
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bioRxiv - Microbiology 2022Quote: ... Whole-genome sequencing was performed using a next-generation sequencer (MiSeq system; Illumina Inc., San Diego, CA, USA). The obtained NGS reads were mapped to the SARS-CoV-2 Wuhan-Hu-1 reference genome sequence (29.9 kb single-strand RNA ...
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bioRxiv - Genomics 2023Quote: The list of the 100 publicly available ovine whole genome sequences (WGS, short read Illumina HiSeq/Nova Seq) coming from 14 different breeds generated in various INRAE and Teagasc research projects is detailed in Table S1 (project and sample accession numbers) ...
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bioRxiv - Microbiology 2023Quote: All DH10B transconjugants used as donors were also verified by whole-genome sequencing (Illumina paired-end 300bp reads), to verify that only the target plasmid and no other MGEs were transferred ...
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bioRxiv - Evolutionary Biology 2023Quote: ... Whole genome sequencing was performed on Illumina HiSeq 4000 or Illumina Novaseq 6000 platforms (Illumina, San Diego, CA) with generation of 150 bp paired-end reads.
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bioRxiv - Microbiology 2023Quote: We performed whole-genome sequencing (WGS) of the 158 barcoded strains used in our study (200 Mbp Illumina DNA sequencing ...
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bioRxiv - Genetics 2023Quote: We analyzed the whole genome sequences of 1,869 cattle from more than 70 different breeds generated by Illumina technology (Supplementary Table 14) ...
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bioRxiv - Evolutionary Biology 2019Quote: ... (Sacramento, CA) for whole-genome 150 bp paired-end sequencing on a NovaSeq 6000 (Illumina Inc., San Diego, CA). Between 59,765,048 and 74,464,410 paired reads were obtained for each sample ...
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bioRxiv - Neuroscience 2020Quote: ... nDNA was extracted from whole blood and genotyped on Illumina GWAS arrays for ADNI1 (Illumina Human 610-Quad BeadChip), ADNI GO/2 participants (Illumina HumanOmniExpress BeadChip) ...
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bioRxiv - Evolutionary Biology 2020Quote: ... The whole genome (WGS) for each pool was sequenced in a Miseq platform (Illumina, Inc., San Diego, CA, USA) at the Molecular and Cellular Imaging Center at the Ohio State University.
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bioRxiv - Microbiology 2020Quote: ... whole-genome sequencing was carried out using the Illumina HiSeq2500 genome analyser (Illumina HiSeq 2500 platform, Illumina, Essex, UK). The reads were assembled to contigs using SPAdes.
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bioRxiv - Evolutionary Biology 2021Quote: ... the strains were previously subjected to whole-genome shotgun sequencing using 2×250bp Illumina paired-end reads (Illumina, USA). Genomes were assembled using SPAdes (v ...
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bioRxiv - Evolutionary Biology 2021Quote: We genotyped all individuals from the central transect for a selection of 1,152 SNPs spread across the whole genome using the GoldenGate assay (Illumina). A detailed description of the assay design ...
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bioRxiv - Genomics 2022Quote: ... Whole genome sequencing (WGS) of the prepared libraries was performed through Illumina MiSeq sequencer (Illumina, San Diego, CA, USA) using a 2 × 250 paired-end protocol.
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bioRxiv - Microbiology 2022Quote: ... Whole genome DNA was paired-end sequenced (2 × 150 bp) using Illumina NovaSeq 6000 (Illumina, San Diego, CA, USA) at Shanghai Personal Biotechnology Co. ...
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bioRxiv - Microbiology 2022Quote: Library for whole genome sequencing was prepared using Nextera™ DNA Flex Library Prep (Illumina; San Diego, CA, USA) as per the recommended protocol ...
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bioRxiv - Microbiology 2022Quote: ... Paired-end sequencing (2×150 bp) and PCR-free whole genome sequencing was performed on a HiSeq X (Illumina) 54 ...
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bioRxiv - Evolutionary Biology 2023Quote: ... (2022) sequenced 20 vaquita porpoise (Phocoena sinus) whole genomes from the Gulf of California to 60x coverage (Illumina HiSeqX). They mapped reads to the vaquita reference genome (mPhoSin1.pri ...
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bioRxiv - Microbiology 2023Quote: ... and the samples were subjected to Illumina-based whole-genome sequencing using a MiSeq 250 paired-end run (Illumina). CLC Genomics Workbench (Qiagen ...
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bioRxiv - Cancer Biology 2023Quote: ... samples were sequenced for low-pass whole genome sequencing with at least 0.1X coverage in a NovaSeq 6000 (Illumina).
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bioRxiv - Microbiology 2022Quote: ... and libraries prepared using the NexteraXT kit and sequenced using HiSeq 1 × 150-cycle v3 kit (Illumina). The operational taxonomic unit (OTU ...
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bioRxiv - Immunology 2020Quote: ... 0.1 ng of cDNA from each cell on the plate was individually tagmented using the Nextera XT kit (Illumina, San Diego, CA) in a final volume of 5 µl ...
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bioRxiv - Pathology 2021Quote: ... The single nucleotide polymorphisms (SNPs) in BRSK2 gene region were genotyped by Infinium Asian Screening Array and Infinium Multi-Ethnic Global BeadChip (Illumina, Inc., San Diego, CA, USA), and SNPs passed through quality-control procedure (individual call rate >98% and approved with Hardy-Weinberg equilibrium ...
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bioRxiv - Genetics 2021Quote: ... RADseq libraries and whole genome libraries were prepared and sequenced on the HiSeq 3000 or NovaSeq S2 sequencing system (Illumina). RADseq sequencing data were analyzed as described in the linkage map section ...
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bioRxiv - Genomics 2020Quote: Whole-genome shotgun sequencing of the DNA extracts was performed on the Illumina NextSeq 500 instrument (Illumina, San Diego, CA) using a modified Illumina Nextera library preparation protocol as described previously [30] ...
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bioRxiv - Molecular Biology 2019Quote: ... Those strains were chosen in order to genotypically match NSTI strains on the basis of micro-array-deduced clonal complexes (23) confirmed by whole genome sequencing (Illumina MiSeq technology ...
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bioRxiv - Molecular Biology 2019Quote: ... Those strains were chosen in order to genotypically match NSTI strains on the basis of micro-array-deduced clonal complexes (23) confirmed by whole genome sequencing (Illumina MiSeq technology, Illumina, San Diego ...
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bioRxiv - Microbiology 2021Quote: ... Whole-genome sequencing (WGS) using a multiplex sequencing approach was performed on an Illumina Miseq genome sequencer (Illumina, Cambridge UK) using Nextera XT libraries and third generation MiSeq reagent kits ...
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bioRxiv - Neuroscience 2020Quote: ... Bulk DNA samples and single neuronal nuclei amplified by multiple displacement amplification (MDA) were prepared and whole-genome sequenced by Illumina HiSeq platforms as part of previous studies in our lab (16) ...
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bioRxiv - Genomics 2019Quote: A set of 196 strains was subjected to whole genome shotgun sequencing using 2×250 bp Illumina (Illumina, Inc., USA) paired-end reads by MicrobesNG (https://microbesng.uk/ ...
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bioRxiv - Microbiology 2020Quote: ... The pO157-cured and WT strains were whole genome sequenced from a paired-end library to generate short-read (Illumina) sequences (ENA accessible number ...
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bioRxiv - Microbiology 2021Quote: ... 2008 [60] and the whole genomes sequenced on the HiSeq2000 according to the manufacturer’s instructions (Illumina, San Diego, CA, USA) at the Welcome Trust Sanger Institute ...
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bioRxiv - Genomics 2019Quote: ... A whole genome library was created from strain CAI4-F2-Neut5L-NAT1-mCherry-GFP using Nextera-XT library construction strategy(Illumina) and sequenced on an Illumina MiSeq (150×150 paired end sequencing ...
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bioRxiv - Evolutionary Biology 2019Quote: We used whole genome amplification of single miracidia dried on FTA cards followed by exome capture and sequencing (Illumina 2500) to generate genome-wide sequence data following methods described in Le Clec’h et al ((Le Clec’h ...
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bioRxiv - Genetics 2021Quote: ... and ultra-deep whole genome sequencing (average 30X read-depth across the genome) was performed on a HiSeq X Ten System (Illumina). We developed an efficient data processing and quality control pipeline ...
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bioRxiv - Genetics 2021Quote: ... high-throughput exome sequencing was performed on a whole-exome library created from Tvrm266 genomic DNA on a HiSeq 2000 Sequencing System (Illumina) as previously described [98] ...
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bioRxiv - Neuroscience 2020Quote: ... and ultra-deep whole genome sequencing (average 30X read-depth across the genome) was performed on a HiSeq X Ten System (Illumina). We developed an efficient data processing and quality control pipeline ...
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bioRxiv - Microbiology 2022Quote: ... was combined with short-read whole-genome sequencing data for the 169 individuals (2×125 bp or 2×150 bp Illumina paired-end sequencing ...
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Human CCR6+ Th cells show both an extended stable gradient of Th17 activity and imprinted plasticitybioRxiv - Immunology 2023Quote: ... Arrays were washed and scanned following the protocols in the Illumina Whole-Genome Gene Expression Direct Hybridization Assay Guide (Illumina). Signal data were extracted from the image files with the Gene Expression module of the GenomeStudio software (Illumina ...