Labshake search
Citations for Illumina :
251 - 300 of 9263 citations for 2'3' Cyclic GAMP cGAMP 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 - 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 - 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 - 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 - 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 - 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 ...
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bioRxiv - Molecular Biology 2023Quote: ... was used to prepare a whole-transcriptome sequencing library and sequenced on one lane of a NovaSeq 6000 SP (Illumina) machine.
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bioRxiv - Cancer Biology 2023Quote: ... 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 tumour ...
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bioRxiv - Plant Biology 2023Quote: ... together with a wild type (WT) plant were whole genome sequenced with an Illumina sequencer (Illumina Inc., San Diego, USA). One μg of DNA was used to prepare short insert (length 350 bp ...
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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 2019Quote: We generated a whole-genome paired-end library with the Illumina TruSeq DNA Sample Prep v2 (Illumina, San Diego, CA, USA), selecting for a mean fragment length of 450 bp with the SPRIselect reagent kit (Beckman Coulter ...
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bioRxiv - Microbiology 2021Quote: ... Whole-genome sequence determinations of strain CS1 were carried out with the PacBio (Pacific Biosciences, USA) and Illumina MiSeq (Illumina, USA) sequencing platform ...
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bioRxiv - Genomics 2020Quote: Whole-genome DNA methylation measurement was performed on DNA from purified CD4+ T cells using Infinium MethylationEPIC BeadChip (Illumina 850K array) by the Center for Applied Genomics Genotyping Laboratory at the Children’s Hospital of Pennsylvania ...
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bioRxiv - Microbiology 2021Quote: ... Whole-genome sequencing was performed by GATC Biotech (Konstanz, Germany) with paired-end libraries on an Illumina HiSeq platform (Illumina, USA) generating reads of 151bp in length.
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bioRxiv - Cancer Biology 2023Quote: With the exception for Whole Transcriptome Amplification Analysis (WTA)7 (sent to Novogene and sequenced on a S4 flowcell of an Illumina Novaseq), all single-cell or bulk sequencing was prepared as ready-made libraries and sequenced either on Illumina Novaseq or Nextseq 500 instruments at the Functional Genomics Center Zurich ...
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bioRxiv - Genomics 2023Quote: ... The genome of TY-11 was sequenced using a whole-genome (WGS) strategy (30-fold genome coverage) with NextSeq 550 (Illumina, USA).
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bioRxiv - Genomics 2024Quote: The DNA samples were submitted to the Centre Nacional d’Anàlisi Genòmica (CNAG-CRG, Barcelona, Spain) for whole-genome sequencing on a NovaSeq 6000 instrument (Illumina, San Diego, CA, USA) in paired-end mode ...
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bioRxiv - Cancer Biology 2020Quote: ... with MiSeq Reagent Kit V3 (150 cycle) (Illumina, MS-1-2-3001). The sequencing data was de-multiplexed and trimmed to contain only the sgRNA sequence cassettes ...
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bioRxiv - Molecular Biology 2024Quote: ... 0.003 μl Tagmentation DNA Enzyme 1 (TDE1; Illumina DNA sample preparation kit) to the 1μl of diluted cDNA per well ...
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bioRxiv - Plant Biology 2023Quote: ... cDNA libraries were constructed from 1 μg/sample of total RNA using library preparation kits (NEBNext Ultra II RNA Library Prep Kit for Illumina 7770L ...
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bioRxiv - Genetics 2021Quote: We converted the published set of 13,037,955 loci (derived from whole-genome short-read Illumina sequencing using Illumina HiSeq 2000 by [33]) into VCF format ...
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bioRxiv - Microbiology 2022Quote: ... 1 ng of genomic DNA from each sample was converted to whole-genome sequencing libraries using the Nextera XT sequencing reagents according to the manufacturer’s instructions (Illumina, San Deigo CA).
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bioRxiv - Genomics 2021Quote: ... whole-genome of each strain was sequenced using Illumina NextSeq 2×150 bp after NextEra XT library preparation (Illumina, San Diego, CA) as in de Lastours et al ...
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bioRxiv - Plant Biology 2021Quote: ... Whole genome resequencing and bisulfite sequencing were performed on the extracted genomic DNA using the Illumina X-ten platform (Illumina, California, USA). Short-insert (350 bp ...
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bioRxiv - Biophysics 2022Quote: ... Whole-genome sequencing was performed on the Illumina NovaSeq platform using Truseq ChIP-seq library and protocols (Illumina, San Diego, CA, USA) with a minimum Phred quality score of 30 ...
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bioRxiv - Microbiology 2020Quote: ... and the samples were prepared for whole genome sequencing according to Nextera® XT DNA Library Preparation Guide (Illumina Inc., Madison, Wisconsin). After the PCR clean up-step ...