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Citations for Illumina :
151 - 200 of 686 citations for Family With Sequence Similarity 46 Member B FAM46B Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Molecular Biology 2023Quote: ... Raw sequence data (.bcl files) generated from Illumina were converted into fastq files and de-multiplexed using Illumina bcl2fastq 2.20 software ...
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bioRxiv - Cancer Biology 2024Quote: ... Raw sequence data (.bcl files) generated from Illumina HiSeq was converted into fastq files and de-multiplexed using Illumina’s bcl2fastq 2.20 software ...
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bioRxiv - Cell Biology 2024Quote: ... Raw sequence data (.bcl files) determined from Illumina HiSeq was converted into fastq files and de-multiplexed using Illumina’s bcl2fastq 2.17 software ...
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bioRxiv - Immunology 2023Quote: ... Raw sequence data (.bcl files) generated from Illumina NovaSeq was converted into fastq files and de-multiplexed using Illumina bcl2fastq 2.20 software ...
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bioRxiv - Cell Biology 2024Quote: ... Raw sequence data (.bcl files) generated from Illumina HiSeq was converted into fastq files and de-multiplexed using Illumina’s bcl2fastq 2.17 software ...
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bioRxiv - Cancer Biology 2024Quote: ... Raw sequence data (.bcl files) generated from Illumina NovaSeq was converted into fastq files and de-multiplexed using Illumina bcl2fastq program version 2.20 ...
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bioRxiv - Biochemistry 2020Quote: ... and 1 μL of 0.25 μM primer (RTB000 and RTB001 in Table S5 for the no modification and 1M7 samples respectively, with these sequences adding an index sequence and Illumina adapter). The reaction volume was brought to 15 μL ...
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TAD border deletion at the Kit locus causes tissue-specific ectopic activation of a neighboring genebioRxiv - Genetics 2022Quote: Raw paired-end reads were preprocessed with Cutadapt tool to trim adapter sequences (-a and -A flags with Illumina adapter sequences)78 ...
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bioRxiv - Genomics 2020Quote: ... sequencing reads were mapped to reference viral genome sequence and consensus sequence for each sample was built using Dragen RNA pathogen detection software (version 9) in BaseSpace (Illumina Inc, USA). For amplified whole-genome sequencing ...
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bioRxiv - Evolutionary Biology 2022Quote: ... although sequence data for each isolate is derived from pools of individuals (except from PCR-free Illumina sequence data for S. avenae), all individuals sequenced for a given isolate are expected to contain the same two haplotypes and so sequence data can be combined to reconstruct fully phased haplotypes for each isolate.
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bioRxiv - Neuroscience 2021Quote: Raw reads were obtained from BaseSpace Sequence Hub (Illumina). Sickle was used with the default parameters to perform quality control and produce trimmed reads 57 ...
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bioRxiv - Neuroscience 2021Quote: ... the resulting sequences were demultiplexed using bcl2fastq v2.19 (Illumina) and trimmed of their indexing adaptors using Trimmomatic v0.32 (Bolger ...
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bioRxiv - Plant Biology 2019Quote: The single-end sequence fragments (reads) generated by Illumina sequencing were base-called and demultiplexed ...
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bioRxiv - Immunology 2019Quote: ... The adaptor sequences for 16S metagenomic library preparation (Illumina) were added to the 5□ ends of the primers designed ...
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bioRxiv - Plant Biology 2020Quote: ... we analysed 16S rRNA gene sequences (Illumina MiSeq platform) recovered from publicly available and newly generated data on seagrass roots and sediments across 14 seagrass species and 10 countries (Fig ...
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bioRxiv - Microbiology 2022Quote: ... The sequences of viral stocks were confirmed by Illumina HiSeq 2500 sequencing.
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bioRxiv - Molecular Biology 2020Quote: ... Sequence images were transformed using the software BaseCaller (Illumina) to obtain BCL files ...
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bioRxiv - Neuroscience 2021Quote: Raw reads were stored in BaseSpace Sequence Hub (Illumina) and downloaded to the University of Connecticut High Performance Computing cluster ...
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bioRxiv - Genomics 2021Quote: ... Nucleotide sequences were obtained with a MiSeq instrument (Illumina) in the paired-end 301 bp mode ...
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bioRxiv - Genomics 2021Quote: ... These regions were replaced by sequences assembled from Illumina reads by SPAdes version 3.12 (60) ...
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bioRxiv - Developmental Biology 2021Quote: ... Amplicon sequence analysis was performed by using MiSeq (Illumina), and the preparation of DNA libraries and sequencing reactions were performed according to the manufacturer’s instructions ...
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bioRxiv - Molecular Biology 2022Quote: ... to assay individual sequences and/or sequenced by Illumina (Centre d’expertises et de services Genome Québec) ...
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bioRxiv - Genomics 2022Quote: ... We demultiplexed the resulting sequences using bcl2fastq2 v2.20 (Illumina). We then discarded low-quality reads and trimmed reads to 61 by removing heterogeneity spacers ...
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bioRxiv - Plant Biology 2023Quote: FASTQ file generation from Illumina sequences was performed by CASAVA software v1.8.2 (Illumina Inc.). Illumina sequences were further filtered for low quality at a score of 20 using Sickle v1.33 [10] ...
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bioRxiv - Systems Biology 2023Quote: The sequence data were demultiplexed using bcl2fastq software (Illumina). RNA sequence data were processed using CELseq2 pipeline 58 which includes demultiplexing based on cell barcodes ...
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bioRxiv - Microbiology 2024Quote: ... The sequence reads (Illumina, paired-end, 150 cycle reads) for the suppressor strains were imported into Geneious Prime (v ...
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bioRxiv - Cancer Biology 2024Quote: ... Sequence libraries were multiplexed and sequenced on NovaSeq (Illumina).
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bioRxiv - Genomics 2021Quote: ... reporter cDNA was PCR amplified using a reporter specific forward primer and a reverse primer binding the anchor sequence of the oligo- dT primer (corresponding to the Illumina TruSeq Read 1 sequence):
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bioRxiv - Zoology 2020Quote: ... but with TruSeq DNA Single Indexes (Set B, Illumina), following the manufacturers’ instructions up till the adapter ligation step ...
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bioRxiv - Systems Biology 2019Quote: ... Set B: indexes 13–24 (Illumina, RS-200-0024), Set C ...
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bioRxiv - Cell Biology 2020Quote: ... and TruSeq RNA Single Indexes Set B (20020493, Illumina) according to standard Illumina library preparation procedure ...
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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 - Genetics 2021Quote: BAM files containing alignments of DGRP line sequences from Illumina platforms to the y ...
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bioRxiv - Cell Biology 2019Quote: ... Sequences were produced using NextSeq and/or HiSeq chemistry (Illumina). Cluster generation on NextSeq 500 followed the instructions of the manufacturer ...
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bioRxiv - Plant Biology 2019Quote: The RNA-Seq and Iso-Seq sequences generated from Illumina and PacBio RS II sequencing of four tissue samples of S ...
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bioRxiv - Plant Biology 2021Quote: Transcriptomic RNA-Seq Sequence Read Archive (SRA) studies (Illumina sequencing) from fruit/flower and leaf tissue samples were downloaded ...
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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 - Molecular Biology 2022Quote: ... Library preparation was done using cDNA and sequences by Illumina platform ...
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bioRxiv - Microbiology 2022Quote: ... DNA was extracted and the sequence was verified by Illumina next-generation sequencing (NGS).
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bioRxiv - Pathology 2022Quote: ... Sequences were determined by HiSeq2000 (Illumina, San Diego, California, USA) as 100-bp paired-end runs ...
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bioRxiv - Microbiology 2019Quote: ... All representative sequences of the OTUs (from pyrosequencing and Illumina) were checked again for chimeras with the DECIPHER v 2.0 program (http://www2.decipher.codes/FindChimeras.html ...
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bioRxiv - Cell Biology 2019Quote: Pre-processing: raw sequence data (.bcl files) generated from Illumina HiSeq was converted into fastq files and de-multiplexed using Illumina’s bcl2fastq 2.17 software ...
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bioRxiv - Genomics 2019Quote: ... the sequence 3’ of the indices were bound by Illumina’s Sequencing Primers ...
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bioRxiv - Molecular Biology 2021Quote: ... Raw reads containing adapter sequences were trimmed using bcl2fastq (Illumina), and nucleotides with low-quality (QV < 25 ...
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bioRxiv - Molecular Biology 2021Quote: Demultiplexed reads were downloaded from the BaseSpace Sequence Hub (Illumina). Most analysis steps were carried out using the RNAFramework RNA structure probing analysis toolkit92 ...
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bioRxiv - Immunology 2021Quote: ... and productive in-frame junction sequences were paired by Illumina read ID and compiled by CDR3 nucleotide and V(D)J gene identity ...
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bioRxiv - Evolutionary Biology 2020Quote: We aligned paired-end sequence data (Illumina HiseqX 150 PE) from five female and five male great reed warbler individuals to the reference genome (sample information in Supplementary Table 1b) ...
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bioRxiv - Microbiology 2019Quote: ... The complete sequence of pHT315-PxylA’rapI was verified by Illumina sequencing (MGH DNA Core ...
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bioRxiv - Microbiology 2020Quote: BCl2fastq was used to convert raw sequence reads from Illumina NextSeq to fastq format ...
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bioRxiv - Genomics 2020Quote: ... and SNPs with poor sequence quality (Illumina phred score < 20) were removed ...