The largest database of trusted experimental protocols
> Living Beings > Mammal > Canis lupus

Canis lupus

Canis lupus, commonly known as the gray wolf or timber wolf, is a large canine species native to North America and Eurasia.
This apex predator plays a crucial role in maintaining the balance of ecosystems, regulating populations of prey species.
Canis lupus exhibits a wide range of behaviors, from pack hunting to solitary scavenging, and adapts to diverse habitats, from tundra to forests.
Understanding the biology, ecology, and conservation status of this iconic species is essential for effective wildlife management and preserving biodological diversity.
Researchers can leverage PubCompare.ai's AI-powered solutions to streamline their Canis lupus studies, locatiing the most reliable and effective research protocols from published literature, pre-prints, and patents.

Most cited protocols related to «Canis lupus»

We have updated the PicTar miRNA target site predictions to the respective UCSC genome releases of man (hg18), mouse (mm9) and worm (ce6). PicTar 2.0 (7 (link)) predicts miRNA target sites in 3′ UTRs and utilizes multiple genome sequence alignments to boost its precision. Briefly, all 3′ UTR alignments for a given species set are scanned for perfect and imperfect seed sequences. Perfect seeds consist of a 7 nt perfect match starting at position 1 or 2 from the 5′-end of a mature miRNA. Imperfect seeds contain one insertion/deletion or mismatches to the 3′ UTR sequence. All candidate sites are subject to probabilistic scoring by an Hidden Markov Model (HMM).
For example, human miRNA targets for mature and star sequences from Mirbase v16 were predicted based on UCSC's 44-way Vertebrate Genome alignment. We have incorporated three conservation levels for human target sites into doRiNA: (i) Mammals, chicken and fish—seed conservation across Pan troglodytes, Mus musculus, Rattus norvegicus, Canis lupus, Gallus gallus, Fugu rubripes and Danio rerio. (ii) Mammals, chicken—seed conservation is not required in Fugu rubripes and Danio rerio. (iii) Mammals—seed conservation is not required in Gallus gallus, Fugu rubripes and Danio rerio.
These conservation levels provide a convenient way to choose the optimal sensitivity level while controlling for false positives.
Publication 2011
Canis lupus Chickens Fishes Genome Helminths Homo sapiens Hypersensitivity INDEL Mutation Mammals Mice, House MicroRNAs Pan troglodytes Patient Discharge Rattus norvegicus Sequence Alignment Takifugu rubripes Vertebrates Zebrafish
A ML tree from whole-genome SNP data was constructed using SNPhylo (Lee et al. 2014 (link)). SNPhylo transforms genotype data into a structured data array (Bioconductor gdsfmt) and then generates and aligns SNP sequences and constructs the phylogenetic trees. The program was run with 100 bootstrap repetitions, and only one outgroup was used (Israeli golden jackal) due to the software's internal limitations.
PCA was performed using the pairwise allele-sharing genetic distance. Following vonHoldt et al. (2011) (link), sites exhibiting apparent strong local linkage disequilibrium (R2 > 0.5) were filtered using the --indep option in PLINK (--indep 50 5 0.2) (Purcell et al. 2007 (link)). To improve resolution among wolves, the two golden jackals and coyote were removed from the PCA because they were too divergent from dogs and wolves, and their inclusion compressed the scatter among wolves on the first few PCs. The lower coverage genomes (<10-fold; Inner Mongolia wolf 2, Eastern Russian wolf, and Yellowstone wolf 3) were also removed due to their potential high genotype error (Supplemental Fig. S5). Additional PCA was also performed excluding one Tibetan wolf and one Qinghai wolf based on the observation that highland Chinese wolves were similar to one another but were highly divergent from all other wolves (Zhang et al. 2014 (link)). Finally, additional PCAs were performed with samples from specific geographic regions, such as Asia or Europe, and including only gray wolves. In both tree analyses and PCAs, we excluded the Yellowstone wolf 2 because it is the offspring of Yellowstone wolf 1 (mother) and Yellowstone wolf 3 (father).
Publication 2016
Alleles Birth Canis familiaris Canis lupus Chinese Coyotes Genome Genotype Jackals Mothers Trees Wolves
DNA from thirteen species was used as PCR template (Table 2). The target species and size of the PCR insert (excluding primers) were as follows: impala (Aepyceros melampus) 92 bp; grey wolf (Canis lupus) 91 bp; cheetah (Acinonyx jubatus) 91 bp; hippopotamus (Hippopotamus amphibious) 91 bp; lion (Panthera leo) 95 bp; saiga antelope (Saiga tartarica) 93 bp, Mueller's Bornean gibbon (Hylobates muelleri) 94 bp, narwhal (Monodon monoceros) 90 bp; domestic mouse (Mus domesticus) 97 bp; musk ox (Ovibos moschatus) 93 bp; human 94 bp; Burchell's zebra (Equus burchelli) 89 bp; and African buffalo (Syncerus caffer) 94 bp. The DNA was extracted from frozen specimens using the DNEasy tissue extraction kit (Qiagen) following the manufacturer's protocol. To increase the number of different PCR products that we could pool into the GS20-reaction beyond a single product from each of available thirteen extractions, we used individual primer pairs on several different extractions each (Table 2).
Full text: Click here
Publication 2007
Antelopes Buffaloes Canis lupus Cheetahs Freezing Gibbons Hippopotamus Homo sapiens Mice, House Monodon monoceros Mus domesticus musk Negroid Races Oligonucleotide Primers Panthera leo Syncerus Tissues Wolves Zebras
Genomic DNA was isolated from blood samples of domestic dogs (Canis familiaris, n = 912) and from tissue and blood samples of grey wolves (C. lupus, n = 225) and coyotes (C. latrans, n = 60; see Supplementary Methods and Supplementary Table 1). The samples were genotyped and quality control filters were applied (see A.R.B. et al., manuscript submitted) to obtain high-quality genotypes from 48,036 autosomal SNP loci.
Publication 2010
BLOOD Canis familiaris Canis lupus Coyotes Genome Genotype Lupus Vulgaris Tissues
Blood samples from 256 dogs and seven Apennine wolves (Table 1) were collected following the European Rules for Animal Welfare when collected in Italy and approved National Human Genome Research Institute (NHGRI) Animal Care and Use Committee protocols when collected or received in the United States. The dog populations represent 23 breeds or varieties of historical Italian origin. The ENCI recognizes 13 of these populations as purebreeds and nine of which are also recognized by the AKC. Ten populations are termed “varieties,” and represent regional homogeneous populations, generally managed by informal registries and maintained by owners for specific behavioral applications. Three breeds, the Cane Corso, Italian Greyhound, and Neapolitan Mastiff, were sampled from Italian populations to compliment a preexisting collection of American populations of the same breeds. Animals selected for analysis were as distantly related as possible based on pedigree information from ENCI. DNA extraction was performed with the commercial Qiagen DNeasy Blood & Tissue Kit. Samples were genotyped on the Illumina CanineHD bead chip (Illumina, San Diego, CA, USA), which contains 172,115 potential markers, in the Ostrander laboratory at the National Human Genome Research Institute (NHGRI) of the National Institutes of Health (Bethesda, MD, USA) using manufacturer's recommended protocols.
Genotyped samples were merged with a larger dataset of 1,346 dogs representing 161 breeds (described in (Parker et al., 2017)) and publically available genotypes from five New Guinea Singing Dogs and three Catahoula Leopard Dogs (Hayward et al., 2016) to produce a dataset of 1,609 dogs representing 182 breeds, seven Apennine wolves, seven global Grey wolf representatives, and two Golden Jackals.
Full text: Click here
Publication 2018
Animals BLOOD Breeding Canes Canis familiaris Canis lupus DNA Chips Europeans Genotype Jackals Leopard Population Group Tissues Wolves

Most recents protocols related to «Canis lupus»

A total of 1,054,293 dogs (811,628 mixed breed and 242,665 purebred dogs) were successfully genotyped as a part of this study. All DNA samples were voluntarily submitted for commercial genetic testing (Wisdom Panel, MyDogDNA, and Optimal Selection Canine genetic screening products) by Wisdom Panel (Portland, OR, USA) between November, 2019 and August, 2021. The relatedness status of dogs was unknown at the time of sample submission. The study cohort represented a subset of the total more than 3.5 million dogs of varying ancestry genetically tested at Wisdom Panel since the service launch. A total of 1,086,817 samples were first selected based on having been genotyped on the largest available cross-compatible microarray technology platform and 32,524 (3%) of them were excluded due to not passing our routine quality control metric for genotyping (sample-specific call rate >0.97%). The country of origin of each dog was defined as the country where the sample was submitted for genetic analysis, unless specific information stating otherwise was reported by the owner. A total of 160 countries or autonomous regions were represented in the dataset (96 regions with >5 dogs). The vast majority of dogs (93.9%) were from the United States, with other notable subgroups being dogs from the United Kingdom (2.5%), Germany (1.2%), France (0.5%), Australia (0.3%), Finland (0.2%), and Canada (0.2%).
As one major motivation for clients to pursue Wisdom Panel genetic testing is gaining insight into their dog’s breed ancestry, the purebred status of a dog was either not known or considered prior to genotyping. Breed assignment was based on comparison to a reference panel of over 21,000 dogs of known ancestry from more than 50 countries and ascertained using the BCSYS Local Ancestry Classifier algorithm [61 ]. For the purposes of this study, a dog was considered “purebred” if its genetic testing results indicated at least 7 of 8 great-grandparents being purebreds of the same breed. Notably, we did not strive to use a definition of “purebred dog” synonymous with the term “pedigreed dog” in terms of eligibility for registration with a recognized kennel club or breed registry. The purebred cohort (S2 Table) consisted of 263 different breeds or breed varieties (218 breeds represented by >5 dogs) and 34 samples from wild canids (gray wolves, dingos, and coyotes). Breeds contributing more than 2% of individuals of the overall study sample were: American Staffordshire Terrier (17.6%), Labrador Retriever (6.9%), German Shepherd Dog (6.4%), French Bulldog (5.4%), Golden Retriever (5.3%), Siberian Husky (3.7%), Yorkshire Terrier (3.4%), Shih Tzu (3.1%), Border Collie (2.8%), Pomeranian (2.2%), Beagle (2.2%), Pug (2.1%), Chihuahua (2.2%), and Standard Bulldog (2.0%).
Full text: Click here
Publication 2023
Breeding Canidae Canis lupus Coyotes Eligibility Determination Grandparent Microarray Analysis Motivation Proteins Reproduction
The SNP genotype data generated by the iScan system were loaded into the Illumina GenomeStudio program to perform the primary data analysis and generate a final custom report (PED and MAP) for downstream analysis. Data obtained from the 39 Tazy were merged with publicly available SNP array data of 89 dogs from seven sighthound breeds and 14 Gray Wolves downloaded from the Dryad repository (datadryad.org, doi:10.5061/dryad.v9t5h; doi:10.5061/dryad.pm7mt). The sample code and corresponding breed are listed in S3 Table. In the PLINK 1 (www.cog-genomics.org/plink/1.9/) [25 (link)] Input Report, 166,171 SNPs of the 89 samples from seven breeds and 14 Gray Wolves and 172,115 SNPs of the 39 samples from the Tazy dogs were filtered using the following steps: (1) removal of very closely related individuals PI_HUT > 0.4; (2) filtering of SNPs that have an exact Hardy-Weinberg equilibrium (—hwe 0.01); (3) removal of SNPs on the X and Y chromosomes (—not-chr); (4) selection of only SNPs with minor allele frequency (—maf) > 0.05; (5) calling rate SNP (—geno) 0.05; (6) removal of SNPs with pairwise genotypic associations (r2) > 0.2 within a window of 50 SNPs (—indep-pairwise 50 5 0.2). The number of SNPs retained for calculations after the filtering process was 40,229 autosomal SNPs. The PCoA of unrelated dogs was performed using PLINK 1.9 software and visualized in the R package "ggplot2" [26 , 27 (link)].
Full text: Click here
Publication 2023
Breeding Canis familiaris Canis lupus Genotype Single Nucleotide Polymorphism Y Chromosome
Samples were collected from three different areas, including two natural sites and one anthropized site located in Tuscany, Central Italy (Figure 1).
The anthropized site (Area 1) is located in Pisa Province within the municipalities of Crespina Lorenzana and Casciana Terme Lari (10.56815° N–43.56796° E) and includes 18 towns, with an average human density of 134.08 people/km2. The area is characterized by a highly anthropized fragmented agroecosystem in which small woody areas are interspersed with agricultural and urban zones [9 (link)]. A wide variety of wild mammals live in this area, such as crested porcupines (Hystrix cristata), wild boars (Sus scrofa), roe deer (Capreolus capreolus), pine martens (Martes martes), stone martens (Martes foina), skunks (Mustela putorius), badgers (Meles meles), hares (Lepus europeus), eastern cottontails (Sylvilagus floridanus), wild rabbits (Oryctolagus cuniculus), red foxes (Vulpes vulpes), wolves (Canis lupus), and the introduced invasive coypu (Myocastor coypus) [10 (link)].
The natural area includes two different sites: the Monterufoli Caselli Nature Reserve of (Val di Cecina, Pisa, Central Italy, 43°15′6.48″ N, 10°45′26.64″ E) (Area 2) and the Foreste Casentinesi National Park (43°50′36″ N 11°47′28″ E) (Area 3). The Monterufoli Caselli Nature Reserve covers an area of 4.978 ha and is characterized by wide woody areas of Mediterranean scrub and oaks (Quercus ilex). Hares; wild ungulates (mainly wild boars, fallow deer (Dama dama), and mouflons (Ovis musimon)); and carnivores such as red foxes, wolves, pine martens, weasels (Mustela nivalis), badgers, stone martens, and wild cats (Felis silvestris silvestris) are the most representative wild mammals in the area [11 ]. The Foreste Casentinesi National Park (43°50′36″ N 11°47′28″ E), which extends along the Tuscan-Romagna Apennine Ridge [12 ], is characterized by a great richness and variety of wild fauna. The most common mammals are the red deer (Cervus elaphus), the fallow deer, the roe deer, wild boars, mouflons, and the wolf, the largest predator present in the park. At least 21 species of micro- and meso-mammals have been observed in the park territory, among which the most common are the fox, the wild cat, the hare, the European mole (Talpa europaea), the blind mole (Talpa caeca), the red squirrel (Sciurus vulgaris), the crested porcupine, and the raccoon (Procyon lotor), as well as several mustelid species, such as badgers, weasels, stone martens, skunks, and martens.
Full text: Click here
Publication 2023
Badgers Blindness Calculi Canis lupus Carnivora Cecum Deer Europeans Felidae Felis Hares Homo sapiens Hystrix Mammals Martes Mephitidae Moles Mouflon Mustela putorius Mustelidae Oryctolagus cuniculus Pinus Porcupines Quercus Quercus ilex Raccoons Sheep Squirrels Sus scrofa Vulpes vulpes Weasels Wolves
The gray wolf optimization algorithm (GWO) is a pack intelligence optimization algorithm designed by Mirjalili [54 (link)]. It was inspired by the social stratification characteristics and hunting and trapping behavior of wolves. It has the advantages of strong convergence performance, a simple structure, and easy implementation. There exist convergence factors with self-adaptive adjustment and information feedback mechanisms. Thus, a balance between local optimization and global optimization is achieved. For this reason, it has good problem-solving accuracy. Gray wolves are divided into four social classes: α, β, δ, ω . After sorting according to the adaptation function, α wolves represent the optimal solutions. β wolves and δ wolves represent the suboptimal solutions, with their role to assist α wolves in making decisions. The remaining candidate solutions are defined as ω wolves. Classes of α wolves, β wolves, and δ wolves command the hunting behavior, and ω wolves follow the above-mentioned higher-level wolves in hunting. Since the position of the prey (the optimal solution) in the solution space is not known, it is assumed that the positions of wolf α , wolf, and wolf δ are closest to the prey.
As shown in Figure 8 [54 (link)], the hunting process of the gray wolf surrounding prey is represented by the following mathematical model: D=|CXP(t)X(t)|
X(t+1)=Xp(t)AD
where C and A are coefficient vectors determined by random values, Xp(t) and X(t) represent the position vector of the prey and the position vector of the gray wolf at iteration up to the t-th generation, respectively [54 (link)]. Since the location of the optimal solution in the solution space is not known, it is assumed that the locations of wolf α , wolf β , and wolf δ are closest to the optimal solution. After recording the positions of these three wolves, the ω wolf is ordered to approach the α wolf, and the β wolf is ordered to approach the δ wolf. During each iteration, the positions of the α wolf, the β wolf, and the δ wolf are updated via the formulae shown in Equation (12) [54 (link)]: Dα=|C1XαX|    Dβ=|C2XβX|    Dδ=|C3XδX|
X1=XαA1(Dα)    X2=XβA2(Dβ)    X3=XδA3(Dδ)
Averaging the positions of the α wolf, the β wolf, the δ wolf, and the result obtained is regarded as the final position after this iteration is updated. When |A|<1 in Equation (12), the next generation of gray wolves can be located anywhere near the prey. The constant repetition of this behavior is to hunt the prey. It is worth mentioning that in order to prevent falling into local optimal solutions during the optimization process, the gray wolf chooses to move away from the prey when |A|>1 .
To enable the gray wolf optimization algorithm to perform multi-objective optimization, Mirjalili provided two components [55 (link)]. One is a storage component responsible for storing non-dominated Pareto optimal solutions, which implements the storage function of several optimal solutions. The other is a leader-selection strategy component, which can obtain dominance relations with the help of the Pareto global optimum concept but cannot compare solutions that are not dominated by each other. This component selects a new leader in the uncrowded region of non-dominated solutions according to the roulette wheel method, marked as α, β, δ , which is then archived.
In this study, two objective functions were chosen as constraints and the expressions are as shown in Equation (14): Minimize:f1(x)=PMinimize:f2(x)=HI     x=[x1,x2,,x6]T,x(xL,xU)
where P and HI represent the random forest HI prediction model and the random forest indentation pressure generation prediction model, respectively, xi(i=1,2,,6) represents the i-th design parameter, and xL and xU are the upper and lower bounds of each design parameter, respectively. All codes in this paper were written in the MATLAB environment, the number of populations in each iteration was set to 100, and the maximum number of external archives was chosen to be 100, for a total of 400 iterations, running on a PC with Inlet(R) Core(TM) i7-12700 k CPU 5.00 GHz 32 GB RAM.
Full text: Click here
Publication 2023
Acclimatization calcium phosphate, dibasic, dihydrate Canis lupus Cloning Vectors Population Group Pressure Wolves
The overall optimization process for the blood pump is divided into three parts (Figure 1). The first step is the creation of a random forest prediction model. First, the parameters and boundary values controlling the impeller shape are determined. Then, 240 sets of impeller parameters are randomly obtained using the Latin hypercube sampling method, and a 3D model is built and numerically simulated to obtain a database consisting of impeller parameters and pressure generation, and HI values. Thereafter, the random forest prediction model is trained. The second part is multi-objective optimization, using the multi-objective gray wolf optimizer (MOGWO) to calculate the Pareto front. This involves selecting three different optimized models in the Pareto front for modeling and performing the numerical simulation. In the third part, the internal flow differences between the baseline model and the optimized model are analyzed, and the model with the best-combined situation is selected. Each step is described carefully in the following section.
Full text: Click here
Publication 2023
BLOOD Canis lupus Forehead Pressure

Top products related to «Canis lupus»

Sourced in United States
The CanineHD BeadChip is a high-density genotyping array designed for comprehensive genome-wide analysis of canine samples. It provides a comprehensive set of genetic markers covering the entire canine genome, enabling researchers to conduct a wide range of genetic studies and analyses.
Sourced in United States, Germany, Australia, Italy
The SuperScript III One-Step RT-PCR System is a laboratory equipment product designed for reverse transcription and polymerase chain reaction (RT-PCR) in a single-tube format. It combines the SuperScript III Reverse Transcriptase and Platinum Taq DNA Polymerase in a simplified workflow.
Sourced in United States, China, United Kingdom, Hong Kong, France, Canada, Germany, Switzerland, India, Norway, Japan, Sweden, Cameroon, Italy
The HiSeq 4000 is a high-throughput sequencing system designed for generating large volumes of DNA sequence data. It utilizes Illumina's proven sequencing-by-synthesis technology to produce accurate and reliable results. The HiSeq 4000 has the capability to generate up to 1.5 terabytes of data per run, making it suitable for a wide range of applications, including whole-genome sequencing, targeted sequencing, and transcriptome analysis.
Sourced in United States, United Kingdom
GenomeStudio software is a data analysis tool designed for Illumina microarray and sequencing platforms. It provides a unified interface to visualize, analyze, and interpret genomic data generated from Illumina instruments.
Sourced in Germany, United States, France, United Kingdom, Netherlands, Spain, Japan, China, Italy, Canada, Switzerland, Australia, Sweden, India, Belgium, Brazil, Denmark
The QIAamp DNA Mini Kit is a laboratory equipment product designed for the purification of genomic DNA from a variety of sample types. It utilizes a silica-membrane-based technology to efficiently capture and purify DNA, which can then be used for various downstream applications.
Sourced in United States, United Kingdom
The M220 Focused-ultrasonicator is a laboratory instrument designed for sample preparation using focused acoustic energy. It is capable of disrupting the cellular structure of samples, enabling efficient extraction and analysis of biomolecules such as DNA, RNA, and proteins.
The BioSprint 96 DNA Blood Kit is a nucleic acid extraction system designed to purify DNA from whole blood samples. The kit utilizes magnetic particle technology to efficiently capture and isolate DNA, providing a reliable and high-quality DNA extraction solution for a variety of downstream applications.
Sourced in United States, Japan, United Kingdom, Germany, Austria, Belgium
SPSS Statistics version 20 is a comprehensive software package for statistical analysis. It provides a wide range of statistical procedures and techniques for data management, analysis, and presentation. The software is designed to handle a variety of data types and can be used for tasks such as descriptive statistics, regression analysis, and hypothesis testing.
Sourced in United States, Germany, Australia, Japan, United Kingdom, Netherlands, France, Canada, Switzerland, Spain
The 3130xl Genetic Analyzer is a capillary electrophoresis instrument designed for DNA sequencing and fragment analysis. It features 16 capillaries and a laser-induced fluorescence detection system. The 3130xl enables high-throughput genetic analysis with its automated sample handling and data processing capabilities.

More about "Canis lupus"

The gray wolf, also known as the timber wolf or Canis lupus, is a large, iconic canine species found in North America and Eurasia.
As an apex predator, the gray wolf plays a vital role in maintaining the balance of ecosystems, regulating the populations of its prey species.
This remarkable animal exhibits a wide range of behaviors, from pack hunting to solitary scavenging, and is adaptable to diverse habitats, from tundra to forests.
Understanding the biology, ecology, and conservation status of the gray wolf is crucial for effective wildlife management and preserving biodiversity.
Researchers can leverage advanced tools and technologies to streamline their Canis lupus studies.
The CanineHD BeadChip, for example, provides a high-density genotyping array for in-depth genetic analysis of the gray wolf and other canine species.
The SuperScript III One-Step RT-PCR System can be used for sensitive and reliable gene expression studies, while the HiSeq 4000 platform and GenomeStudio software enable comprehensive genomic sequencing and analysis.
The QIAamp DNA Mini Kit and BioSprint 96 DNA Blood Kit are valuable tools for efficient DNA extraction from gray wolf samples, and the M220 Focused-ultrasonicator can be used for effective DNA fragmentation.
Statistical analysis of gray wolf data can be performed using software like SPSS Statistics version 20, and the 3130xl Genetic Analyzer can be employed for high-resolution genetic profiling.
By leveraging these cutting-edge tools and technologies, researchers can enhance the reproducibility and accuracy of their Canis lupus studies, leading to a deeper understanding of this iconic species and informing its conservation efforts.
PubCompare.ai's AI-powered solutions can further streamline the research process, helping scientists locate the most reliable and effective protocols from published literature, pre-prints, and patents.