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Citations for Illumina :
1 - 50 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 - Genetics 2020Quote: ... A genome-wide analysis genotyping scan was performed in all six members of family A and in the proband of family B using the HumanCytoSNP-12 DNA Analysis BeadChip Kit (Illumina, San Diego), according to manufacturer’s instruction ...
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bioRxiv - Genomics 2019Quote: ... was applied to remove low quality sequences (i.e. four consecutive bases below Phred 15) and remaining adapter sequences (based on similarity to all known Illumina adapter sequences). Different sets of trimmed reads were subjected to SOAPdenovo2 (Luo et al ...
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bioRxiv - Genetics 2023Quote: ... The IBD between long-lived family members was calculated using the --ibd module from Merlin using previously generated genome-wide genetic data from Illumina BeadChips 72.
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bioRxiv - Immunology 2019Quote: ... The B-cell repertoire sequences consist of 150bp non-overlapping paired-end reads (Illumina MiSeq), with one read covering much of the V gene and the other read covering the area around the CDR3 region and the J gene ...
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bioRxiv - Genomics 2023Quote: ... for each sample using Illumina protocol25 and the PE150bp strategy were used to sequence the 16S Metagenomic Sequencing Library following protocol (Part # 15044223 Rev. B) of MiSeq 2500 platform (Illumina). The amplified 16S gene by PCR was resolved in a 1.5% agarose gel.
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bioRxiv - Molecular Biology 2020Quote: ... or phiX sequences as the control sequence from Illumina were removed using Bowtie 2 v ...
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bioRxiv - Systems Biology 2023Quote: ... The resulting sequences were uploaded to Illumina Sequence Hub and downloaded using BaseSpace Sequence Hub Downloader (Illumina).
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bioRxiv - Evolutionary Biology 2019Quote: Sequences from Illumina were analyzed in PyRAD v ...
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bioRxiv - Genomics 2019Quote: ... For HapMap samples and three PGT-M families paired-end (2×125bp) sequencing was performed on a HiSeq2500 system (Illumina) in multiple runs ...
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bioRxiv - Microbiology 2020Quote: ... The number of exported cells was estimated on family-level by first multiplying 16S rRNA gene abundances per liter by the seepage volume collected at a given time point and by the relative abundance of a given family obtained from Illumina amplicon sequencing ...
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bioRxiv - Microbiology 2022Quote: ... with methods for library preparation and sequencing as previously described (46) or by Illumina short read WGS by MicrobesNG (University of Birmingham ...
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bioRxiv - Molecular Biology 2021Quote: ... Adapter sequences were based on the TruSeq small RNA sequences (Illumina), with an additional seven random nucleotides at the 5′-end of the 3′-adapter and the 3′-end of the 5′-adapter ...
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bioRxiv - Pathology 2021Quote: ... Adapter sequences were based on the TruSeq small RNA sequences (Illumina) and ...
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bioRxiv - Genomics 2019Quote: ... The Rd2SP sequence (Illumina) was introduced downstream of the kanamycin resistance for sequencing purposes ...
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bioRxiv - Cancer Biology 2021Quote: ... Sequence adapters (Illumina TruSeq) were trimmed using Trimmomatic v0.39 [40] at the following settings ...
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bioRxiv - Evolutionary Biology 2019Quote: ... finished sequences from Illumina de novo assemblies of L ...
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bioRxiv - Evolutionary Biology 2021Quote: Representative sequences from Illumina and Sanger methods were evaluated using BLAST searches of the NCBI nucleotide (nt) ...
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bioRxiv - Cell Biology 2021Quote: ... The corrected long-read sequences from MinION and short-read sequences from Illumina Miseq were hybrid de novo assembled using rnaSPAdes v3.14.1 (75)(https://cab.spbu.ru/software/rnaspades/ ...
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bioRxiv - Microbiology 2022Quote: ... B provided by Illumina technical support ...
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bioRxiv - Genetics 2022Quote: ... The primers sequences were modified to include Illumina Nextera index PCR adaptor sequences (Illumina).
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bioRxiv - Microbiology 2021Quote: ... Sequences were determined by Illumina and assembled using Newbler and Consed ...
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bioRxiv - Genomics 2020Quote: ... to sequence on HiSeqX (Illumina). The size of the 'Aogashima-1' genome was estimated using Jellyfish v2.1.411 ...
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bioRxiv - Plant Biology 2019Quote: Sequence read information from Illumina HiSeq 2000 2×100 PE fastq files were used as input for the CLC Bio Genomic Workbench (ver 6.0.1)(Aarhus ...
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bioRxiv - Microbiology 2022Quote: ... Raw sequence reads from Illumina were submitted to the NCBI Sequence Read Archive ...
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bioRxiv - Microbiology 2022Quote: ... and phyloFlash sequences from Illumina metagenomes ...
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bioRxiv - Molecular Biology 2023Quote: ... Sequences were identified by Illumina base calling software then aligned to the reference genome using Bismark ...
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bioRxiv - Evolutionary Biology 2023Quote: ... Adapter sequences published by Illumina and BGI were used for trimming ...
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bioRxiv - Evolutionary Biology 2021Quote: ... short-read sequence data (either 100-bp or 150-bp paired-end Illumina sequence data) with SPAdes v3.11.1 and default settings (Bankevich et al. ...
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bioRxiv - Microbiology 2020Quote: The reference genome sequence was required to obtain the complete sequence of MrV40L by Illumina Miseq ...
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bioRxiv - Microbiology 2022Quote: ... which is designed to resolve exact biological sequences (ASVs for Amplicon Sequence Variants) from Illumina sequence data without sequence clustering (Callahan et al ...
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bioRxiv - Microbiology 2021Quote: ... 8) DC3000 − B (Illumina only), 9 ...
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bioRxiv - Microbiology 2021Quote: ... 4) DC3000 + B (Illumina only), 5 ...
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bioRxiv - Synthetic Biology 2021Quote: ... DNA sequence was confirmed by Illumina MiSeq Sequencing V2 and V3 chemistry.
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bioRxiv - Genomics 2020Quote: ... to sequence on a HiSeqX (Illumina). From the sequence reads obtained ...
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bioRxiv - Cancer Biology 2021Quote: Sequence data was obtained from Illumina HiSeq paired-end sequencing ...
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bioRxiv - Synthetic Biology 2021Quote: ... Raw sequence data 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 2021Quote: ... and sequences were generated by Illumina HiSeq 2000 and MiSeq systems with read lengths of 93nt and 251nt ...
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bioRxiv - Microbiology 2020Quote: ... To sequence 16S amplicons by Illumina MiSeq platform ...
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bioRxiv - Microbiology 2022Quote: ... Raw sequence data generated from Illumina HiSeq was converted into fastq files and de-multiplexed using Illumina’s bcl2fastq 2.17 software ...
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bioRxiv - Molecular Biology 2020Quote: ... sequence data from the NextSeq500 (Illumina) was demultiplexed ...
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bioRxiv - Genomics 2022Quote: The raw sequences generated by Illumina Hiseq2000 were further filtered based on reproducibility average values ...
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bioRxiv - Physiology 2023Quote: ... and sequences were obtained by Illumina MiSeq via the Next Generation Sequencing Core in the Biosciences Division at Argonne National Laboratory (Walters et al ...
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bioRxiv - Microbiology 2023Quote: Demultiplexed raw sequence data from Illumina HiSeq/MiSeq were resolved to amplicon sequence variants (ASVs ...
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bioRxiv - Cell Biology 2023Quote: ... Barcode sequences were extracted from Illumina sequence reads after removing common sequences around the barcodes ...
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bioRxiv - Genomics 2023Quote: Sequences were demultiplexed using bcl2fastq (Illumina) filtering for reads with RT and ligation barcodes within an edit distance of 2 bp ...
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bioRxiv - Systems Biology 2023Quote: ... We extracted sgRNA sequences from Illumina FASTQ files using regular expressions ...
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bioRxiv - Microbiology 2023Quote: ... Adapter sequences were trimmed from Illumina sequencing reads using Trimmomatic v0.39 ...
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bioRxiv - Cancer Biology 2024Quote: ... Raw sequence data generated from Illumina NextSeq 500 were converted to FASTQ files and Quality control analysis was performed on fastq files using FastQC (https://www.bioinformatics.babraham.ac.uk/projects/fastqc/) ...
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bioRxiv - Genomics 2021Quote: ... Minimap2 44 was used to align the MinION read sequences to the gene sequences derived from Illumina sequences obtained in our previous transcriptome analyses 12 to the contigs ...
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bioRxiv - Genomics 2021Quote: 71| Annotate any remaining ambiguities in the clone sequence (e.g., unresolved simple sequence repeats, where neither Illumina or nanopore reads are completely accurate ...