Sequence variation of 16S rRNA gene primer-binding sites.

Slides:



Advertisements
Similar presentations
The Build-up of the Red Sequence at z
Advertisements

Molecular Genetics DNA RNA Protein Phenotype Genome Gene
Genomic walking (1) To start, you need: -the DNA sequence of a small region of the chromosome -An adaptor: a small piece of DNA, nucleotides long.
DNA Questions What makes up a DNA backbone? How would you describe how DNA looks? Name the 4 bases that make up DNA. “T” base can only match with? What.
22 kDa a-coixin gene cluster
Rearrangements of Gene A and Gene B
Sequence variation in the promoter region of the cholinergic receptor muscarinic 3 gene and asthma and atopy  Joseph Donfack, PhDa, Paul Kogut, BSb, Sean.
Alternative Computational Analysis Shows No Evidence for Nucleosome Enrichment at Repetitive Sequences in Mammalian Spermatozoa  Hélène Royo, Michael Beda.
Cg-OxyR oxidation decreases binding affinity and extension to the catalase promoter region. Cg-OxyR oxidation decreases binding affinity and extension.
The 5′‐terminal structure of the miRNA gene cluster miR‐23a∼27a∼24‐2.
Phosphorylation and sequence disorder in microtubule-associated protein Tau.A, schematic illustration of the domain profile of Tau with all known phosphorylation.
Volume 38, Issue 4, Pages (May 2010)
M Rollandet al. Nature 000, 1-4 (20120) doi: /nature11519
(A) Schematic representation of kalata B1 showing the cyclic cystine knot, the amino acid sequence in single letter code, and the regions used for oligonucleotide.
Evolutionary dynamics of UQ FMOs in the proteobacterial lineage.
The dicBF locus is conserved in E. coli species in different prophages
Q-Q plot of observed P values against theoretical P values for factor analysis (red dots) and single gene–based methods (in blue). Q-Q plot of observed.
Volume 6, Issue 6, Pages (December 2000)
Alignment of H-NS, H-NS2, and StpA amino acid sequences.
Fractions of 16S rRNA genes from bacteria (top panel) and archaea (bottom panel) in public databases from primer-amplified metagenomes (with and without.
Phylogenetic relationships between representatives of the Bacteroidetes “Candidatus Amoebophilus” (based on 1,218 bp) and amplicon SSU rRNA gene sequences.
Trans-Splicing to Spliceosomal U2 snRNA Suggests Disruption of Branch Site-U2 Pairing during Pre-mRNA Splicing  Duncan J. Smith, Charles C. Query, Maria.
Representative RAPD profiles from pools of H
Transcription levels of metabolic pathways and genes in mother and infant pair 4 at time point 2. Transcription levels of metabolic pathways and genes.
Correlation of mouse gene expression with bacterial gene expression.
Parallel evolution of coding sequences above neutral expectation.
Comparison of the variable regions of (A) pHNZY32, pHNZY118, and pHNAH24; (B) pHNMCC14; (C) pHNFKU92; (D) pE80; (E) pECB11; (F) p42-2; and (G) pSLK172-2.
Gene-wise Tajima’s D values and gene lengths.
Disease ontology of genes associated with ZIKV-induced changes.
Maximum likelihood (ML) unrooted tree based on the full-length 16S rRNA genes (A) and 31 conserved single-copy genes (B) showing the phylogenetic position.
Example of amplicon performance in our presented workflow.
Genome-wide binding sites of OsMADS1 and the distribution of binding sites in different regions of annotated genes. Genome-wide binding sites of OsMADS1.
Schematic representation of the HAV genome organization, translation products, and regions used for amplification. Schematic representation of the HAV.
Phylogenetic tree of 38 Pseudomonas type strains, based on the V3-V5 region sequence of the 16S rRNA gene (V3 primer, positions 442 to 492; and V5 primer,
Proportion of 16S rRNA gene sequences in each category of phylogenetic novelty relative to cultures for each environment, by amplicons, metagenomes (without.
Protein Synthesis.
16S rRNA gene survey reveals a moderate impact of formula-based B
Relative abundances of Propionibacterium species in different skin areas determined by 16S rRNA gene sequence analysis of 10 individuals. Relative abundances.
Nucleotide sequence alignment of porA gene sequences from the examined English Neisseria gonorrhoeae porA mutants, compared to the porA sequences of previously.
Tagging of the endogenous Py03652 gene with the gfp gene in Plasmodium yoelii. Tagging of the endogenous Py03652 gene with the gfp gene in Plasmodium yoelii.
Framework for integrating taxonomic and metabolomic data.
RNA abundance correlates with fitness.
Diagram of fusion primers and dual-indexing approach for library construction. Diagram of fusion primers and dual-indexing approach for library construction.
dsRBDs 3 and 4 of hStau1 are sufficient for ARF1 SBS binding.
(A) Taxonomic identity at the phylum level of raw leachate (RL) and enrichment microcosms (E) as determined via Ion Torrent 16S rRNA gene amplicon sequencing.
Core genome phylogeny of V. anguillarum strains.
Linear schematic of the basic quality control procedure for marker gene (microbiome) data. Linear schematic of the basic quality control procedure for.
Schematic representation of the domain structures of insect enzymes involved in chitin metabolism. Schematic representation of the domain structures of.
Comparison of Nonpareil Nd sequence diversity and 16S rRNA gene OTU Shannon H′ taxonomic diversity indices on 90 metagenomes. Comparison of Nonpareil Nd.
The Bov-A2 element is conserved in the NOS2 gene of bovid species.
(A and B) Unweighted (A) and weighted (B) UniFrac clustering of three 16S rRNA hypervariable regions using fragment insertion SATé-enabled phylogenetic.
Strong parallelism in mutated genes defines adaptations to the environment of CF patient lungs. Strong parallelism in mutated genes defines adaptations.
Fig. 5 E2F1 also interacts with alternatively spliced transcripts from the MECOM gene. E2F1 also interacts with alternatively spliced transcripts from.
Principal-coordinate analysis (PCoA) (Hellinger distance metric) of plant community (A), soil chemistry (B), 16S rRNA gene (prokaryotic) (C), and ITS (fungal)
Schematic map of the X and Y chromosomes
Expression of selected intergenic regions in response to increasing concentrations of XIP. qRT-PCR analysis of gene expression was performed with strain.
ITS rRNA gene locus. ITS rRNA gene locus. Schematic of the eukaryotic ribosomal gene cluster. The SILVA database contains sequences of the 18S gene, while.
Comparison of gut microbiota alpha diversity in different preservatives based on 16S rRNA gene V3-V4 amplicon sequencing. Comparison of gut microbiota.
Purification scheme. Purification scheme. (A) Line drawing of CelTag fragment from CelTag plasmid. PCR (polymerase chain reaction) of fragment was performed.
Nucleotide sequences of the IS1016-bexAdeletion region of type b strain Hib and type a strains 1, 2, and 5. Nucleotide sequences of the IS1016-bexAdeletion.
Mutation of the Ca2+ Channel β Subunit Gene Cchb4 Is Associated with Ataxia and Seizures in the Lethargic (lh) Mouse  Daniel L Burgess, Julie M Jones,
P-network of 2,616 prokaryote genomes based on chromosomal sequences with rRNA genes removed. P-network of 2,616 prokaryote genomes based on chromosomal.
Identification of chromatin modifying complex recruiting H3K9 methyltransferases. a, A MEME-ChIP analysis was performed to identify the transcription factor.
Comparison of the frequency of nucleotide variation in the mtDNA D-loop region between stomach and other tumor cell lines. Comparison of the frequency.
16S rRNA gene profiling of D
Splice isoforms of the JNK1, JNK2, and JNK3 proteins.
Schematic representation of the HPV genome, highlighting the regions important in PCR-based HPV analysis. Schematic representation of the HPV genome, highlighting.
Tree depicting the phylogenetic relationships of all strains included in this study. Tree depicting the phylogenetic relationships of all strains included.
Differences in the relative abundances of mycobacteria (as determined via 16S rRNA gene sequencing) across households in the United States on municipal.
Fig. 3 Genome editing of the MSTN gene.
Presentation transcript:

Sequence variation of 16S rRNA gene primer-binding sites. Sequence variation of 16S rRNA gene primer-binding sites. (A) Schematic of the 16S rRNA gene regions and primer pairs. (B) Occurrences of the most commonly observed sequences of primer-binding sites and the primer formulations that they may match. Nucleotide sites identical to the most common consensus sequence (the first listed) are represented as dots. The main nucleotide changes of primer sequences from the most common consensus sequence are highlighted in red. Zigui Chen et al. mSystems 2019; doi:10.1128/mSystems.00271-18