Labshake search
Citations for Illumina :
3051 - 3100 of 10000+ citations for Creatinine Serum Low Sample Volume Kit 384 well Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Animal Behavior and Cognition 2022Quote: ... Each sample was sequenced twice in separate sequencing lanes on a HiSeq 4000 sequencer (Illumina) at the Genomic Technology Facility of the University of Lausanne ...
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bioRxiv - Bioengineering 2021Quote: ... The samples were further prepared and analyzed by pair-end next-generation sequencing (Illumina, NextSeq550) carried out at the Center for Gene Research of Nagoya University.
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bioRxiv - Cancer Biology 2020Quote: ... Sample libraries were subsequently pooled and loaded to the Hiseq 2500 (Illumina, serial number SN930). Single end reads at 50bp were generated by using Hiseq rapid SR cluster kit V2 (Illumina ...
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bioRxiv - Cell Biology 2021Quote: ... and the libraries were prepared according to the TruSeq Nano sample preparation guide from Illumina. To generate replication timing profiles ...
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bioRxiv - Neuroscience 2020Quote: ... All remaining samples were processed at Macrogen using TruSeq DNA PCR-Free library preparation (Illumina) followed by minimum 30× sequencing of 7 separate libraries on the Illumina HiSeq X Ten ...
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bioRxiv - Plant Biology 2021Quote: ... as described by the TruSeq RNA sample prep V2 guide (Illumina, San Diego, CA, USA). Size selection was performed using the BluePippin System (SAGE Science ...
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bioRxiv - Microbiology 2020Quote: ... Unique barcodes were added to each sample library using ScriptSeq™ Index PCR Primers (Illumina). Libraries were analyzed on a Tapestation using HS D1000 tapes and reagents (Agilent ...
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bioRxiv - Neuroscience 2021Quote: ... The twelve samples were sequenced according to manufacturer instructions in a HiSeq2500 sequencer (Illumina, Inc). Libraries were strand specific (reverse ...
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bioRxiv - Neuroscience 2021Quote: ... Samples were sequenced on a 50-cycle single end run on a HiSeq 2500 (Illumina) according to manufacturer’s protocols.
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bioRxiv - Neuroscience 2021Quote: ... Samples were sequenced on a 50-cycle single end run on a HiSeq 4000 (Illumina) according to manufacturer’s protocols.
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bioRxiv - Cell Biology 2021Quote: ... Normalized bead intensity data for each sample were loaded into the GenomeStudio software package (Illumina). Ratios of signal intensity were calculated using the Log R Ratio (LRR ...
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bioRxiv - Cell Biology 2020Quote: ... sequenced at a depth of ~ 30 million reads per sample on NextSeq500 Mid Output (Illumina). Raw fastq files were retrieved and processed as follows:
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bioRxiv - Cancer Biology 2022Quote: ... Samples were run with at least 50 million paired-end reads using Novoseq 6000 (Illumina). For mechanistic studies ...
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bioRxiv - Systems Biology 2022Quote: ... Human DNA samples for the COVID study were subjected to the Infinium MethylationEPIC array (Illumina) at AKESOgen Inc. ...
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bioRxiv - Microbiology 2022Quote: PCR reactions were then both combined and cleaned using 1X ratio Sample Purification Beads (Illumina) at a 1:1 bead to sample ratio ...
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bioRxiv - Cancer Biology 2022Quote: ... before samples were submitted for sequencing on a NovaSeq 6000 SP (Illumina, paired-end 150bp), at the CRUK CI Genomic Core Facility.
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bioRxiv - Developmental Biology 2022Quote: ... The samples were then resuspended in 1 ml of ATAC mix (2X TDE buffer (Illumina), 50 µl TDE (Illumina) ...
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bioRxiv - Genomics 2021Quote: ... Samples were sequenced on a HiSeq 4000 next-generation sequencing system (Illumina, San Diego, CA). Sequence reads were aligned to the human reference genome (hg19 ...
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bioRxiv - Neuroscience 2020Quote: ... Samples were loaded at concentrations of 2.7 pM and sequenced on a NextSeq 550 (Illumina) using 1×72 bp reads to an average depth of 40 million reads per sample.
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bioRxiv - Microbiology 2022Quote: ... Sample libraries of sufficient quality were sequenced (Illumina MiSeq; paired end 2 × 75bp read length) with a sequencing depth targeted at 7-10M total paired end reads/sample at the Center for Genome Innovation at the University of Connecticut.
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bioRxiv - Microbiology 2019Quote: ... The RNA samples were sent to the sequencing service for RNA sequencing (RNAseq) by Illumina (Genome Quebec Innovation Center ...
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bioRxiv - Cancer Biology 2019Quote: ... All samples were sequenced on the Illumina HiSeq platform (X/400) (Illumina, San Diego, USA) with 2 × 150bp read length ...
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bioRxiv - Genetics 2019Quote: ... cDNA libraries were constructed following the protocol “Preparing samples for sequencing of mRNA” from Illumina Inc ...
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bioRxiv - Genetics 2020Quote: ... and standard sample preparation protocols and RNA-seq was performed on a Hiseq2000 machine (Illumina) at the NKI Genomics Core Facility ...
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bioRxiv - Molecular Biology 2020Quote: ... Samples were diluted and mixed with 5-20% phiX control v3 (Illumina FC-110-3001) and sequenced with oSK326 for read 1 and oSK324 for the index read.
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bioRxiv - Pharmacology and Toxicology 2019Quote: ... Prepared libraries for all 8 samples were pooled and sequenced on a NovaSeq 6000 (Illumina) using 2×96 paired end reads to capture sample index ...
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bioRxiv - Genomics 2020Quote: ... DNA samples underwent sequencing on an Illumina HiSeq X Ten sequencer (v.2.5 chemistry, Illumina) using 150 bp ...
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bioRxiv - Genomics 2021Quote: ... RNA libraries were constructed in accordance with the TruSeq Stranded mRNA Sample Preparation Guide (Illumina). Nucleotide sequences were obtained with a MiSeq instrument (Illumina ...
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bioRxiv - Genomics 2021Quote: ... Samples were demultiplexed either onboard Illumina HiSeq2500 or offline using bcl2fastq Conversion Software v1.8.4 (Illumina). The quality of raw reads in FASTQ format was checked using FASTQC22 (Supplementary Fig ...
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bioRxiv - Biochemistry 2020Quote: ... The sample was submitted to one channel of Illumina flow cell and sequenced by Illumina Genome Analyzer (GAII ...
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bioRxiv - Microbiology 2021Quote: ... MERS-CoV samples were treated with RiboZero H/M/R rRNA (Illumina, San Diego, CA) depletion mix following the manufacturer’s instructions ...
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bioRxiv - Microbiology 2021Quote: ... Sequencing of the samples was carried out on a NextSeq 500 High Throughput platform (Illumina) for 300 cycles.
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bioRxiv - Immunology 2021Quote: ... Indexed samples were sequenced using the 75 bp paired-end protocol via the NextSeq500 (Illumina) per the manufacturer’s protocol ...
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bioRxiv - Cancer Biology 2021Quote: Total RNA from 18 samples were sequenced in a NextSeq 500 sequencer (Illumina, CA, USA) producing 23,830,047 raw 75 × 2 nt paired-end reads on average ...
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bioRxiv - Genomics 2021Quote: ... Transposition reaction mix containing transposition buffer and 2.5 ul of Tn5 enzyme per sample (Illumina) was added to the pellet and incubated for 30 min at 37 C ...
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bioRxiv - Genetics 2020Quote: ... The samples were sequenced on a total of 8 lanes using a HiSeq3000 instrument (Illumina) with a single end flowcell for 75 cycles ...
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bioRxiv - Physiology 2022Quote: ... Samples were sequenced on the HiSeq 2500 (Figure 2) or NovaSeq 6000 (Figure 6; Illumina) using a 2×100 kit to a read depth >45 million reads/sample ...
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bioRxiv - Microbiology 2022Quote: ... Samples were pooled in equimolar concentrations and sequenced on a MiSeq platform (Illumina, CA, USA) using the V3 ...
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bioRxiv - Cancer Biology 2022Quote: ... Paired-end 50-bp sequencing (50 million reads per sample) was performed using HiSeq (Illumina). Sequencing reads were filtered for Q>15 and trimmed of adapter sequences using TrimGalore (v0.4.5) ...
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bioRxiv - Cancer Biology 2022Quote: ... RNA samples were analyzed using Human HT expression BeadChip V4 (Illumina, San Diego, CA, USA). Raw data were processed using the bead array package from Bioconductor (16) ...
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bioRxiv - Immunology 2022Quote: ... Samples were sequenced using 150 bp paired-end reading on a NovaSeq 6000 instrument (Illumina). RNA-sequencing datasets from P25 RPE obtained from C57BL/6 ...
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bioRxiv - Genetics 2022Quote: ... Benchmarking was performed for the three GIAB samples using Hap.py v3.12.1 (https://github.com/Illumina/hap.py) and v4.2.1 of the NIST benchmarks (21)
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bioRxiv - Genetics 2022Quote: ... Libraries were pooled from different samples based on molar concentrations and sequenced on NovaSeq (Illumina) with 28 bases for read 1 ...
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bioRxiv - Immunology 2022Quote: ... FastQ files for each sample were obtained using bcl2fastq v2.20.0.422 software (Illumina, San Diego, CA). Sequencing reads were aligned to the human reference transcriptome (GRCh38 v91 ...
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bioRxiv - Synthetic Biology 2022Quote: ... adding barcodes to identify the sample (primers P3-P15 in Supplementary Table 3, containing Illumina Nextera tagmentation adapters and ...
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bioRxiv - Synthetic Biology 2022Quote: ... The genomic DNA samples of the mutant strains TP2 and TP4 were sequenced by Illumina HiSeq/Nova 2×150 bp platform ...
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bioRxiv - Neuroscience 2023Quote: ... Samples were subjected to 150 base paired end cycles on the NovaSeq-6000 platform (Illumina). Differential expression analysis was performed by the University of Michigan Bioinformatics Core ...
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bioRxiv - Systems Biology 2022Quote: ... samples were sequenced at a depth of 200M reads on the NovaSeq 6000 platform (Illumina).
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bioRxiv - Molecular Biology 2022Quote: ... and the libraries were prepared according to the TruSeq Nano sample preparation guide from Illumina.
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bioRxiv - Neuroscience 2022Quote: ... Sample libraries were multiplexed and sequenced on a NovaSeq 6000 (Illumina, San Diego, California, US) using paired-end sequencing (150bp ...