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Citations for Illumina :
151 - 200 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 - Cancer Biology 2020Quote: ... the post-PCR whole transcriptome amplification (WTA) products from each single cell were transformed into sequencing libraries using a Nextera XT kit (Illumina) and unique 8-bp DNA barcodes ...
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bioRxiv - Genetics 2021Quote: ... 700 ng of genomic DNA was sheared to an average size of 400 bp using a Covaris LE220 and was used as input to generate a whole-genome library using the TruSeq PCR-free kit (Illumina). The resulting DNA libraries were sequenced on Illumina Hi-seq X instrument to generate 2×150bp paired-end reads.
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bioRxiv - Microbiology 2021Quote: ... cDNA library was prepared by using NEB Next Ultra RNA Library Prep Kit for Illumina (New England Biolab, Cat# E7530) and whole genome sequencing was performed by Miseq (Illumina).
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bioRxiv - Microbiology 2020Quote: ... gDNA was either submitted for sequencing at the Microbial Genome Sequencing Center at the University of Pittsburgh or prepared for whole genome sequencing in house using the Nextera XT DNA Library Preparation Kit (Illumina). Libraries were sequenced using the NextSeq 550 or MiSeq platforms ...
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bioRxiv - Genomics 2022Quote: Whole-genome shotgun libraries of 13 Capsicum lines were prepared with the TruSeq DNA PCR-Free Sample Prep Kit (Illumina), in accordance with the manufacturer’s protocol ...
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bioRxiv - Microbiology 2022Quote: ... tuberculosis genomic DNA was fragmented with a Covaris S220 ultrasonicator and a whole genome library was prepared using the TruSeq Nano library preparation kit (Illumina). Library fragments containing Tn junctions were PCR-amplified from the whole genome library using the Tn-specific primer Mariner_1R_TnSeq_noMm and Illumina p7 primer (Table S6) ...
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bioRxiv - Microbiology 2023Quote: Dual-indexed paired-end libraries for whole genome sequencing were prepared with the Nextera DNA Flex Library Prep Kit from Illumina. Individual libraries were barcoded with Nextera DNA CD Indexes (Illumina ...
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bioRxiv - Bioengineering 2023Quote: ... For 4-week and 8-week organoids cDNA library was prepared by using the whole transcriptome Illumina TruSeq Stranded Total RNA Library Prep Kit Gold (Illumina), followed by evaluation on an Agilent 2100 Bioanalyzer by using the DNA 1000 kit ...
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bioRxiv - Immunology 2023Quote: ... Whole-genome sequencing (WGS) was performed using the Illumina NovaSeq 6000 with the S4 reagent kit (300 cycles) (Illumina, USA) with 2 × 150 bp paired-end reads ...
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bioRxiv - Microbiology 2023Quote: ... tuberculosis gDNA was fragmented with a Covaris S220 ultrasonicator and a whole genome library was prepared using the TruSeq Nano library preparation kit (Illumina). Library fragments containing Tn junctions were PCR-amplified from the whole genome library using the Tn-specific primer Mariner_1R_TnSeq_noMm and Illumina p7 primer (Table S4) ...
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bioRxiv - Genomics 2020Quote: ... on Illumina’s official website (ftp://webdata2:[email protected]/downloads/productfiles/humanomniexpress-24/v1-2/infinium-ommexpress-24-v1-2-mamfest-file-csv.zip) and converted it to a VCF format using Illumina’s GTCtoVCF tool (github.com/Illumina/GTCtoVCF).
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bioRxiv - Developmental Biology 2021Quote: ... Raw sequencing data was demultiplexed and converted to fastq format by using bcl2fastq v2.20 (Illumina, San Diego, CA). Fragment analysis of indexed libraries was performed on the Agilent 4200 TapeStation (Agilent Technologies ...
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bioRxiv - Microbiology 2021Quote: Raw data from the Illumina MiSeq was first converted into FASTQ format 2 × 312 paired-end sequence files using the bcl2fastq program (v1.8.4) provided by Illumina. Format conversion was performed without de-multiplexing ...
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bioRxiv - Microbiology 2022Quote: ... Base-calling was done on the instrument using RTA 3.3.4 and the resulting .bcl files were demultiplexed and converted to FASTQ format with tools provided by Illumina Inc. ...
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bioRxiv - Neuroscience 2021Quote: ... Raw base counts were demultiplexed and converted to sample-specific fastq format files using the bcl2fastq program (Illumina) with default parameters ...
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bioRxiv - Microbiology 2019Quote: Reads in the FASTQ format were cleaned up with trimmomatic/0.36[65] to remove sequences originating from Illumina adaptors and low quality reads ...
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bioRxiv - Immunology 2020Quote: ... Raw data from the Illumina MiSeq was first converted into FASTQ format 2□×□312 paired-end sequence files using the bcl2fastq program (v1.8.4) provided by Illumina. Format conversion was performed without de-multiplexing ...
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bioRxiv - Developmental Biology 2023Quote: Raw sequencing data was demultiplexed and converted to fastq format by using bcl2fastq v2.20 (Illumina, San Diego, California). Then reads were aligned to the transcriptome using STAR v2.6.1 (19 ...
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bioRxiv - Microbiology 2024Quote: ... The fluorescent images were processed into sequences and transformed to FastQ format using the Genome Analyzer Pipeline Analysis software 1.8.2 (Illumina). The sequence output was controlled for general quality features ...
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bioRxiv - Microbiology 2024Quote: Raw sequence reads were demultiplexed and converted to FASTQ format at the GGBC facility using Cassava v1.8 (Illumina). Following demultiplexing ...
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bioRxiv - Microbiology 2021Quote: Whole genome sequencing using MiniSeq or HiSeq systems (Illumina) was performed for phylogenetic and MLST analysis ...
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bioRxiv - Microbiology 2022Quote: ... Whole genome sequencing (Illumina 150 bp paired end reads) was performed at The Microbial Genome Sequencing Centre (Pittsburgh ...
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bioRxiv - Microbiology 2022Quote: ... for whole-genome sequencing on a Hiseq X (Illumina).
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bioRxiv - Evolutionary Biology 2023Quote: ... Whole-genome sequencing libraries were constructed using Nextera (Illumina) DNA Flex Library Prep kits ...
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bioRxiv - Cell Biology 2023Quote: ... Whole transcriptome sequencing was performed using NovaSeq6000 platform (Illumina) in a 101 bp single-end mode ...
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bioRxiv - Microbiology 2024Quote: ... whole genome sequenced with paired 150bp reads (Novaseq Illumina).
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bioRxiv - Cancer Biology 2021Quote: ... indexed libraries for human whole genome sequencing were constructed from 1.0 µg gDNA using the TruSeq DNA PCR-Free Library Prep Kit (Illumina, San Diego) according to manufacturer’s instructions ...
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bioRxiv - Molecular Biology 2020Quote: ... Whole genome bisulfite sequencing (WGBS) libraries were generated from the converted samples with the TruSeq DNA Methylation kit (Illumina Cat#EGMK81312). Consistent fragment size distribution of the resulting libraries was assessed via micro-capillary gel electrophoresis on a Bioanalyzer 2100 (Agilent Cat#G2939BA) ...
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bioRxiv - Microbiology 2019Quote: ... RNA was isolated as described above and purified whole RNA was then rRNA depleted using the Ribo-Zero Bacterial rRNA Removal Kit (Illumina Inc.) and concentrated with the RNA Clean and Concentrator-5 kit (Zymo Research Corp ...
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bioRxiv - Genetics 2021Quote: ... sequencing libraries were generated from whole blood-derived fragmented DNA using the TruSeq DNA Nano kit (Illumina, Inc., San Diego, USA) and sequence reads were generated using a HiSeq X Ten1 system (Illumina ...
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bioRxiv - Evolutionary Biology 2020Quote: ... and ∼ 200 bp insertion size libraries were constructed using the Illumina whole transcriptome analysis kit following the manufacturer’s standard protocol (Illumina, HiSeq system). All libraries were then sequenced on the Illumina HiSeq 2000 at the sequencing core facility at Max Planck Institute for Molecular Genetics (Berlin) ...
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bioRxiv - Immunology 2022Quote: ... a multiplexed amplicon-based whole-viral-genome approach using the NEBNext® ARTIC SARS-CoV-2 Library Prep Kit (Illumina®) was employed (New England Biolabs ...
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bioRxiv - Cell Biology 2021Quote: ... Libraries were constructed for performing whole-transcriptome sequencing using the TruSeq RNA Sample Preparation Kit v2 (Illumina, San Diego, CA, USA) and sequenced using the 100-bp paired-end mode of the TruSeq Rapid PE Cluster Kit and the TruSeq Rapid SBS Kit (Illumina).
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bioRxiv - Microbiology 2019Quote: ... The samples were used to generate whole transcriptome libraries using the NextSeq 500 high output kit (Illumina, San Diego, CA, USA) with a NextSeq 2000 sequencing instrument (Illumina) ...
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bioRxiv - Genomics 2022Quote: ... Whole genome bisulfite sequencing libraries were prepared (according to Accel-NGS Methyl-Seq DNA library Kit for Illumina protocol, Swift Biosciences) and sequenced in 150 bp paired-end reads by Novogene company.
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bioRxiv - Plant Biology 2022Quote: ... The RNA-seq libraries were constructed with the Illumina Whole Transcriptome Analysis Kit as the standard protocol described (Illumina, HiSeq system), and were sequenced on the HiSeq 2000 platform ...
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bioRxiv - Microbiology 2023Quote: ... Libraries for whole-genome sequencing (WGS) were built using a TruSeq DNA PCR-Free Low Throughput Library Prep Kit (Illumina, USA) following the manufacturer’s protocol ...
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bioRxiv - Microbiology 2023Quote: ... DNA libraries of each sample were prepared for whole genome sequencing (WGS) using a Nextera XT kit (Illumina, San Diego, CA). Briefly ...
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bioRxiv - Cell Biology 2020Quote: ... Whole genome sequencing was performed with 1 μg of the digested DNA using a HiSeq X Ten Sequencer (Illumina) at Macrogen (South Korea).
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bioRxiv - Genetics 2021Quote: ... the UCSC mm10 mouse reference genome (fasta) and gene annotation (General Transfer Format (GTF)) file were downloaded from Illumina iGenomes (https://sapac.support.illumina.com/sequencing/sequencing_software/iGenome.html) ...
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bioRxiv - Bioengineering 2021Quote: ... The resulting raw sequence data files (.bcl) were converted to the FASTQ format and de-multiplexed with bcl2fastq 2.17 software (Illumina). One mismatch was permitted for index sequence identification ...
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bioRxiv - Developmental Biology 2022Quote: ... Libraries were loaded at a concentration of 1.8 pM and sequenced in an asymmetrical pair-end format in a NextSeq500 instrument (Illumina).
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bioRxiv - Microbiology 2024Quote: ... Sequencing was performed for 32 total samples in MiSeq v2 250 bp paired-end format (Illumina, San Diego, CA).
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bioRxiv - Bioengineering 2020Quote: ... NE and whole genome sequence data was obtained by Illumina paired end sequencing with read sizes of 150 bases ...
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bioRxiv - Genomics 2020Quote: ... Whole-genome methylation assays were done with HumanMethylation450 BeadChips (Illumina), as previously described2 ...
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bioRxiv - Genomics 2020Quote: ... whole-genome sequencing libraries were prepared using NexteraXT reagents (Illumina) and sequenced on an Illumina HiSeq X Ten platform ...
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bioRxiv - Microbiology 2022Quote: ... and whole genome sequencing was performed using a NextSeq500 (Illumina). Data was uploaded to IRIDA (version 19.09.2 ...
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bioRxiv - Genomics 2021Quote: ... 19) and filtered for whole genome fastq data from Illumina instruments with a human sample background ...
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bioRxiv - Cell Biology 2021Quote: ... Mutant worms were then subjected to whole genome sequencing (Illumina). The molecular lesions of hj49 and hj50 in M01G5.3 were confirmed by Sanger sequencing ...
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FTSH3 facilitates complex I degradation through a direct interaction with the complex I subunit PSSTbioRxiv - Plant Biology 2023Quote: ... Whole genome sequencing was done using the HiSeq 2500 (Illumina). Sequencing reads were aligned to the Arabidopsis reference genome (Araport11 ...