Labshake search
Citations for Illumina :
9601 - 9650 of 10000+ citations since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Cancer Biology 2022Quote: ... using the HiSeq SBS Kit v4 (Illumina). An average of 58 million paired reads was generated per sample ...
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bioRxiv - Cancer Biology 2022Quote: ... Paired-end libraries with 2 × 75 bp reads were prepared from the extracted RNA using the TruSeq Stranded total RNA LT Sample Prep (RiboZero Gold, Illumina) using Illumina methodology ...
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bioRxiv - Cancer Biology 2022Quote: ... purified and sequenced on a MiSeq V3 (Illumina). The abundance of each sgRNA was obtained ...
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bioRxiv - Cancer Biology 2022Quote: ... copy number variations (CNV) and mRNA expression (RSEM, Batch normalized from Illumina HiSeq_RNASeqV2) were downloaded and converted into Excel sheets for analysis ...
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bioRxiv - Plant Biology 2022Quote: ... cDNA libraries were prepared from 200ng of total RNA using a TruSeq mRNA Library Prep Kit (Illumina). cDNA libraries were normalized and pooled then sequenced using HiSeq 2500 (Illumina ...
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bioRxiv - Molecular Biology 2022Quote: The Illumina Infinium® human 450k (Illumina, WG-314-10031) and EPIC methylation (Illumina ...
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bioRxiv - Molecular Biology 2022Quote: ... Sequencing libraries were prepared using Nextera DNA Library Prep Kit (Illumina FC-131-1024) following standard manufacturer instructions for amplicon libraries ...
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bioRxiv - Cell Biology 2022Quote: ... with High output Kit v2.5 (150 cycles) for paired-end sequencing according to standard procedure provided by Illumina.
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bioRxiv - Molecular Biology 2022Quote: ... Libraries were sequenced on the HiSeq 2500 instrument (Illumina) and ~40 million 100-nt reads were generated per ChIP sample ...
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bioRxiv - Molecular Biology 2022Quote: ATAC-seq was conducted on 5×104 live cells using Nextera Tn5 transposase (Illumina) as previously described (Buenrostro et al. ...
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bioRxiv - Molecular Biology 2022Quote: ... and TrueSeq RNA Single Indexes (Illumina, 20020492). Deep sequencing analysis were performed in Illumina NextSeq500 platform at Cold Spring Harbor Laboratory NGS Bioinformatics Center ...
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bioRxiv - Molecular Biology 2022Quote: ... Samples were sequenced by paired-end sequencing on a NextSeq 500 (Illumina).
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bioRxiv - Molecular Biology 2022Quote: ... mRNA-enriched libraries were sequenced 75 cycles in a single read mode on the NextSeq-500 System (v2.5 Chemistry, Illumina). Acquired data was trimmed and FASTQ files were aligned using HISAT2 (version 2.1.0 ...
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bioRxiv - Cancer Biology 2022Quote: ... Sequencing libraries were generated with low with input RNA Nextera protocol (Illumina, Nextera DNA Sample Preparation Kit ...
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bioRxiv - Cancer Biology 2022Quote: ... Sequencing reads were demultiplexed using BCL2FASTQ software (Illumina, USA). FASTQ files were aligned to the Human Whole Transcriptome v2.0 panel ...
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bioRxiv - Cancer Biology 2022Quote: ... Then these libraries were sequenced on the Illumina sequencing platform (HiSeqTM 2500 or Illumina HiSeq X Ten) and 125 bp/150 bp paired-end reads were generated.
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bioRxiv - Cancer Biology 2022Quote: ... The libraries were constructed using TruSeq Stranded mRNA LTSample Prep Kit (Illumina, San Diego, CA, USA) according to the manufacturer’s instructions ...
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bioRxiv - Neuroscience 2022Quote: ... 150-bp paired-end RNA sequencing was performed using a NovaSeq 6000 SP flow cell (Illumina, USA).
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bioRxiv - Cancer Biology 2022Quote: ... The library was sequenced using MiSeq (Illumina) in the Genomic & Bioinformatics Core Facility at the University of Notre Dame ...
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bioRxiv - Cancer Biology 2022Quote: The TruSeq SR Cluster Kit HS4000 or TruSeq PE Cluster Kit HS4000 (Illumina, Inc, California, USA) was used for cluster generation using 8 pM of pooled normalized libraries on the cBOT ...
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bioRxiv - Cancer Biology 2022Quote: Raw sequencing data were demultiplexed and FASTQ files were generated using bcl2fastq software (Illumina, v2.20.0.422). FASTQ files were mapped to the GRCm38 mouse reference genome using salmon (v0.7.2)54 and count matrices were constructed with the R package tximport (v1.18.0)55 ...
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bioRxiv - Cancer Biology 2022Quote: Raw sequencing data were demultiplexed and FASTQ files were generated using bcl2fastq software (Illumina, v2.20.0.422). FASTQ files were trimmed using Trimgalore (v0.6.6)65 and mapped to the GRCm39 mouse reference genome using Bismark (v0.22.3)66 ...
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HNRNPA2B1 controls an unfolded protein response-related prognostic gene signature in prostate cancerbioRxiv - Cancer Biology 2022Quote: ... and 75bp paired end sequencing performed to 30M read depth using the NextSeq 500 (Illumina). Reads were aligned to the genome (hg38 ...
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bioRxiv - Microbiology 2022Quote: ... Libraries were loaded on individual flow cell lanes and sequenced at a depth of 400 million reads using a HiSeq X Ten platform (Illumina) at Macrogen (Seoul ...
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bioRxiv - Developmental Biology 2022Quote: ... The library was made according to the manufacturer’s directions for the TruSeq Stranded mRNA LT Sample Prep Kit - set B (Illumina, Cat. No. RS-122-2102). The resulting short fragment library was checked for quality and quantity using the LabChip GX (PerkinElmer ...
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bioRxiv - Cell Biology 2022Quote: ... and sequenced (paired end 150 bp) on a NovaSeq 6000 instrument (Illumina Inc.) to an average depth of 39 million fragments per sample ...
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bioRxiv - Cell Biology 2022Quote: ... Libraries were prepared with an TruSeq mRNA kit (Illumina Inc., San Diego, CA) and sequenced (paired end 150 bp ...
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bioRxiv - Genomics 2022Quote: ... Sequencing was performed on a NextSeq500 instrument (Illumina) (Read1 ...
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bioRxiv - Genomics 2022Quote: ... RNAseq libraries were prepared using the TruSeq Stranded mRNA Library Prep kit (Illumina) following the manufacturer’s instructions and using 100-125 ng of RNA per cell line as input ...
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bioRxiv - Molecular Biology 2022Quote: ... using TruSeq Stranded Total RNA Gold kit per manufacturers’ instructions (Illumina, 20020598). The libraries were then sequenced on an Illumina NovaSeq6000 platform with 2×150 base pair reads (details of statistics given in Figure S1 ...
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bioRxiv - Cancer Biology 2022Quote: ... and sequenced on NextSeq 500 and NextSeq 2000 (Illumina, USA) using pair-end reads (28 cycles for read 1 ...
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bioRxiv - Neuroscience 2022Quote: ... Ribo-Zero Gold (Human/Mouse/Rat) Kit (Illumina; NEBNext® rRNA Depletion Kit (Human/Mouse/Rat)(E6350 ...
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bioRxiv - Evolutionary Biology 2022Quote: ... all the replicates were pooled by sample before purification and to proceed to the further preparation of the library according to the protocol outlined by Illumina (« 16S metagenomic Sequencing Library Preparation ») ...
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bioRxiv - Neuroscience 2022Quote: ... approximately 10 ng of total RNA per sample was used for library construction with the Ultra-Low-RNA-seq RNA Sample Prep Kit (Illumina) and sequenced using the Illumina HiSeq 4000 instrument according to the manufacturer’s instructions for 100bp paired end read runs ...
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bioRxiv - Cancer Biology 2022Quote: ... The final pool was loaded in one lane of an S2 flow cell using the NovaSeq XP protocol (Illumina Inc.) (Figure S3 ...
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bioRxiv - Cancer Biology 2022Quote: ... Cluster amplification and generation of sequencing data were performed on the NovaSeq 6000 system (Illumina Inc.) using 2×100 paired-end cycles ...
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bioRxiv - Immunology 2022Quote: ... purified with NucleoSpin Gel and PCR Clean-up kit (Quiagen, cat. 740609.50) and sequenced on the MiSeq platform with a MiSeq 600 cycle v3 kit (Illumina, cat. MS-102-3003).
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bioRxiv - Genetics 2022Quote: ... (2019) and was carried out working from short-read (Illumina) WGS data as follows (also see sequencing_pipeline.txt in the online data) ...
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bioRxiv - Genetics 2022Quote: ... we compared short-read (Illumina) and long-read (Nanopore ...
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bioRxiv - Evolutionary Biology 2022Quote: ... For small RNA sequencing I used the TruSeq Small RNA Sample Preparation Kit (Illumina) to generate the cDNA library using selected constructs of sizes 145 to 160 bp in a 6% PAGE gel ...
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bioRxiv - Neuroscience 2022Quote: ... The adaptor sequence “AGATCGGAAGAGC” (Illumina TruSeq, Sanger iPCR; auto-detected) as well as 3 bp from the 5’ end and 15 bp from the 3’ end were removed ...
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bioRxiv - Cancer Biology 2022Quote: ... and paired-end sequencing was performed on a NovaSeq6000 instrument (Illumina) in the Genomics Shared Resource (University of Colorado) ...
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bioRxiv - Molecular Biology 2022Quote: ... and then run by using paired-end 50 bp sequencing on the Illumina HiSeq 4000 platform (Illumina, San Diego, CA, USA). 10,000 cells were targeted for each sample with a sequencing depth of 20,000 read pairs per cell.
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bioRxiv - Genomics 2022Quote: ... Sequencing was performed by Illumina Novaseq 6000 sequencer (Illumina, San Diego, CA, USA) and NovaSeq 6000 S4 Reagent Kit v1.5 (200 cycles ...
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bioRxiv - Neuroscience 2022Quote: ... and libraries were constructed by using 600 ng of total RNA from each sample and utilizing a TruSeqV2 kit from Illumina (Illumina, San Diego, CA) following the manufacturer’s suggested protocol ...
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bioRxiv - Neuroscience 2022Quote: ... gene body and enhancer regions we have used the MethylationEPIC bead chip arrays (Illumina). Bisulfite conversion of genomic DNA ...
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bioRxiv - Immunology 2022Quote: ... libraries were sequenced by Novaseq 6000 platform running Novaseq 6000 S4 Reagent Kit v1.5 300 cycles (Illumina, 20028312) or NovaSeq XP 4-Lane Kit v1.5 (Illumina ...
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bioRxiv - Immunology 2022Quote: ... or NovaSeq XP 4-Lane Kit v1.5 (Illumina, 20043131).
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bioRxiv - Immunology 2022Quote: ... Libraries were sequenced on NextSeq 500/550 (Illumina, San Diego, CA) with an average sequencing depth of 50,000 reads/cell.
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bioRxiv - Genomics 2022Quote: ... and ELLIPSE OncoArray (Hispanic Ethnicity, 1192 cases/1052 controls on Illumina Consortium-OncoArray ...