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    128 fasta ncbi jobs found, pricing in CAD

    Seeking an experienced bioinformatics tutor to guide me through decoding DNA sequ...in detail. - Focused learning on identifying microsatellites within DNA. - A practical approach to applying Python in analyzing these sequences. Skills and Experience Required: - Expertise in bioinformatics, particularly in DNA sequence analysis. - Strong background in programming with Python, with the ability to teach at a beginner level. - Familiarity with diverse DNA data formats, including FASTA and GenBank. - Patience and excellent teaching skills. This educational session is crucial for my research, and the ideal candidate should be ready to break down complex concepts into an easy-to-understand format. If you have the knowledge and passion for teaching Python and DNA analysis, please submit...

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    The onyy info ive found is on like pubmed, ncbi, etc. I would also like info on the number of addiction chinese herbal patent medicines there are in china since 2000(im guessing around 30)how these patent medicines formulas are found and researched and how you can get prescribed them any and all detailed info on the names, ingredients, etc. From inception to a prescrition getting written. Ive been searching for years and havent been able to find anything besides pubmed, ncbi, etc. Or some people asking on rediit or blulight with no good answees. Ive joined fb groups, reddit, quora, used a chinese seqrch engine and browser and chapgpt and bard. I do hqve thw ingredients for jitai tablet. I think basically youll hqve to speak with someone in china

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    I am looking for someone to help me with my de novo genome assembly project. I I just need a complete guide on how to do this, because I have been stuck. Apparently I need a FASTA file and without it I cannot answer the questions I am given. I have rerun the job four times already but there is no FASTA file. I am willing to provide you with all the information needed, including what I have written this far.

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    I am looking for someone to help me with my de novo genome assembly project. I I just need a complete guide on how to do this, because I have been stuck. Apparently I need a FASTA file and without it I cannot answer the questions I am given. I have rerun the job four times already but there is no FASTA file. I am willing to provide you with all the information needed, including what I have written this far.

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    ...genes, between two conditions or between two different strains. To do that you will need to identify a suitable dataset consisting of libraries of paired-end RNA-seq reads (fastq files), one for each condition/strain. How will you find a dataset? You will either 1) start with a literature search, find a relevant paper and then download the paper's data, or 2) start with a search in EBI-ENA or NCBI-SRA or GEO, find a suitable dataset and then track down the study from which it came. In both cases, you should know what the study is, what its goal and motivation was and what conditions/strains are being compared and why. Once you've found your data, in the beginning, you should have two pairs of fastq files: , , , (R1

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    Fasta is a mobile application for use in public transport precisely for buses. The app function is to pin point exactly the location of the bus and yours and calculate the tine of the trajectory then come up with a pricise time the bus will take to reach you at you bus station location

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    Hi there, I have a budget of $30 and need a simple script that would modify two input files: (attached are examples) to create two output files: Below are the "rules/explanations" 1. The first input file (.fasta file) has the following format: >URS0000000183_853 Faecalibacterium prausnitzii 5S rRNA XUDKDKD >URS00000040A7_1340 Streptococcus porcinus 5S rRNA YDUDIED ... This file is organized into pairs of values: Each odd line contains Name (e.g. ">URS0000000183_853 Faecalibacterium prausnitzii 5S rRNA") Each even line contains the corresponding Value (e.g. "XUDKDKD"). To create file, I need to select only those Names and Values from the file which Names are list in the "#Organism Name" column

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    ...python/R/Linux script that organizes, renames, and summarizes subfolders and files within a master file. Example master file and summary output file is attached. Requirements: Script that performs the following actions: 1. Creates a summary text file of the folders. Updates the file as it performs the actions below. (Length and Reads in Consensus columns are pulled from the first line of the FASTA file modification below. Multuple column flags the line if there are multiple files being processed in a folder.) 2. Looks in each of the primary subfolders for a folder that begins with medaka. if the folder contains one or more of these folders: 2a. Moves the file(s) to a new "Summary" folder, renamed. Ex: -> (ONT01

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    This report should take FASTA file and Amino Acid from NCBI website only. BLAST should be made from NCBI website only. Description should be very detail about the genes taken, including nucleotide position numbers and all steps taken and the discussion on them. further can be discussed in a meeting.

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    Hello, we need to do a simple script in python using the bioinformatics libraries available on GitHub. The main goal is to manage the human Whole Genome Sequence. The flow is simple: 0) Allow user to select the file (fastq file) 1) Check the validity of the file 2) Align the Whole Genome to the standard reference (fasta file) 4) Calculate the "coverage uniformity" 5) Select some specific genes (see attached file) 6) Extract the "letters" of these genes 7) Save them in a JSON. If you got this, write "BIOALGORETICO"

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    I have GeneBank files to be converted to Fasta files. In addition, copy paste the sequences to one Word document. Around 100 files.

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    use one line of code to process a fale named which contains a set of DNA sequences in the fasta format for multiple sra IDS

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    I need to demonstrate the gene expression of the NCBI GEO database using the R program.

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    ...particular environment Competition between two very similar species led to divergence in genetic code Human sub-populations diverged in certain genes in response to varying environmental pressures or randomly as a result of genetic drift in isolated populations Use the online nucleotide (and protein) sequence databases to obtain sequences relevant to your species and trait of interest. Genbank and NCBI BLAST These nucleotide sequences will be used as results to support the hypothesis. Perform (multiple) alignments of the sequences and interpret the results. The results/discussion section should analyze the alignments and trees produced by the queries. The only requirement is that there is at least one tree and one alignment generated included in the final paper. Formatting: This...

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    I needs for me NCBI researchers who is defined this project.

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    ...particular environment Competition between two very similar species led to divergence in genetic code Human sub-populations diverged in certain genes in response to varying environmental pressures or randomly as a result of genetic drift in isolated populations Use the online nucleotide (and protein) sequence databases to obtain sequences relevant to your species and trait of interest. Genbank and NCBI BLAST These nucleotide sequences will be used as results to support the hypothesis. Perform (multiple) alignments of the sequences and interpret the results. The results/discussion section should analyze the alignments and trees produced by the queries. The only requirement is that there is at least one tree and one alignment generated included in the final paper. Formatting: T...

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    I need help to Write C++ to load and process DNA sequences in Fasta format. I will provide more details in chat.

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    Genome browse= ) Using the BLAT tool on Ensembl and NCBI BLAST/ RARA protein sequencing

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    Project :Sequence Alignment and Substitution Matrices Input Specs: Allow the user to select peptide (protein, amino acid sequence) or nucleotide sequence files in FASTA format, prompting for the FASTA format filename and sequence type (peptide versus nucleotide). Allow the user to select a matrix of amino acid substitution scores (e.g. BLOSUM, PAM(n), hydrophobicity) in the formats provided in zipped folder P1SubMatrices. You should also allow as input your PAM(n) matrix files, despite the different delimiter format. Notice the amino acid order in all matrices: A,R,N,D,C,Q,E,G,H,I,L,K,M,F,P,S,T,W,Y,V For input nucleotide sequences, you may find the matrix helpful, as it simulates the following nucleotide substitution matrix: A C T G A

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    ...orgamisms, with amino acids, codons (triplets) and respective frequencies. See the example of the standard table attached. ================= As it is explained above, the same protein (amino acid sequence) can be encoded with the various sequences of triplets (codons) of nucleotides. The script should optimize codons in the genes in the following way : INPUT: 1. Gene sequence in a test format (.FASTA) , example attached 2. "Source" Table of the frequencies of codons (triplets) 3. "Target" table of the frequencies of codons (triplets) Script should convert triplets from th gene sequence to amino acid sequence, keeping "in mind" the frequencies of the codons from "Source" table. And then the script should convert the amino acid sequen...

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    ...remedies can help calm patients suffering from anxiety. One of the most effective natural solutions is the use of CBD oil. This is an extract from the hemp plant that effectively treats anxiety’s symptoms, with few to no serious side effects. The adoption of CBD in treating depression and anxiety continues to yield positive results according to continuing research and tests. Recent research by NCBI, the use of CBD to treat sleep-related anxiety disorders registered positive outcomes. These findings are further supported by different research examining the impact of CBD on fear and anxiety. In this second research, CBD proves effective in treating social and general anxiety disorders, especially in post-traumatic stress disorders (PTSD). To appreciate CBD oil treatment'...

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    Trophy icon Design a diagram Ended

    Please design a professional diagr...attached) It needs to show client connecting to Merchant connecting to our Onegate API that will connect them to the below and ultimately up to their Merchant or Bank Account: Acquirers: Absa Bank, FNB, Standard Bank, Nedbank, Bidvest Bank Payment Gateways: PayU, Wirecard, Onegate, Peach Payments, Iveri, Ecentric, Paygate APM's: EFTsecure, 1ForYou, OTT, Blu Voucher, Zapper, Snapscan, Mobicred, Fasta, Payflex, Masterpass, Discover Miles, eBucks, MTN MoMo, Kazang, Bitcoin I will need each Acquirer, Gateway and APM logo's in - which can be found using Google search. All of them is South Africa based offerings. This is urgent and should still award today. If your design is good, I will guide you to correct mistakes and look forward t...

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    Please see attached word application form. I need a redesign of this in word format as well as .pdf that looks appealing. Under the banks (absa, standard bank, nedbank, fnb) I also need a 5th bank added being Bidvest Bank, see logo attached. Under payment methods I need to replace Luno with just Bitcoin (see logo attached). I also need to add new payment method Fasta (see logo attached). feel free to download better copies of the logo's online

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    Want to build a web-based data analysis platform. Basic idea is the user visits the homepage. There is a prompt saying "click here to upload your data". After uploading, and analys...start: Install on Linux Ubuntu EC2 instance: Environments modules for version control of software bowtie2 QualiMap seqtk samtools R? On the EC2 instance (or S3 bucket), establish permanent folder of reference genomes All RM8376 genomes (20) are present as fasta files Index each genome using bowtie2 (use “bowtie2-build” command). Indexed genomes will have the .bt2 extension. Note that multiple bt2 files will be generated for each genome This only needs to be done once and this folder should contain 20 fasta files and all the corresponding .bt2 files Set ...

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    Want to build a web-based data analysis platform. Basic idea is the user visits the homepage. There is a prompt saying "click here to upload your data". After uploading, and analys...start: Install on Linux Ubuntu EC2 instance: Environments modules for version control of software bowtie2 QualiMap seqtk samtools R? On the EC2 instance (or S3 bucket), establish permanent folder of reference genomes All RM8376 genomes (20) are present as fasta files Index each genome using bowtie2 (use “bowtie2-build” command). Indexed genomes will have the .bt2 extension. Note that multiple bt2 files will be generated for each genome This only needs to be done once and this folder should contain 20 fasta files and all the corresponding .bt2 files Set ...

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    Hi, I'm looking to code a bioinformatic pipeline including: - Downloading data from SRA, ENA, JGI, and NCBI - Four main steps: (1) matching SRA sample to genomes using package Mash, (2) QC preprocessing SRA samples using software FastqPuri (3) Quantifying abundance against matching genome using software kallisto or STAR alternatevely (4) Generating orthology (one-to-one) relationship of genes across all genomes using OrthoFinder2 -One step for result consolidation into a count table The main task is chaining output from one tool as input for the next. Please provide me with a quote. Thanks in advance

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    I have a bunch of articles that need to be written and I will give you the topics. They must be 1500 words and use references when applicable from verified sources like NCBI, studies, not other blogs. English proficiency required.

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    Hello, I have an overdue work related to bioinformatic, (linux) that I need help to understand. If anyone can help with linux bash script. I need to understand using NCBI to find taxon and use linux bash commands to manipulate and create a table using commands like grep, cat, awk, sed, expr, head and cut. I really need help as I falling behind.

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    Hi We need this ad for FB and IG We want the fare zone to be as the picture we uploaded. It should be with Vectors and the main road only visible just like the image (see image 300) The zones should not be over the sea as in the picture (image 1). We need following text to be in the picture: Fasta billiga priser dygnet runt! (Gäller ej fre & lör 15.00-07.00) Use the following url for zones The colours of the zone should be the same as in Image

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    necesito redactor academico, para elaborar tesis de grado en distintas areas, medicina, ingeniera, enfermeria, psicologia, educacion entre otros, que manejes programas estadisticos como SPSS, Rstudio, entre otros, adecuado uso de las normas, APA VANCOUVER HARVARD; CHICAGO, uso de metodologia PRISMA, gestion de referencias Mendeley, buen manejo de los motores de busqueda y bases de busqueda como pubmed NCBI, Scielo google academy entre otros motores de busqueda , sobre todo responsable

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    Looking for a writer who can do 3 articles per week related to healthcare, skin, dermatology and AI technology. Articles need to read well and use links to pubmed, ncbi, .org sites for any references. Thanks!

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    Possibly use NCBI databse to find genome sequences. pyhton program to perform genome assembly a 3-4 pages documents describing 1. data collection and method 3. results evaluation It'll be great if you know how to use bioinfo databases like ChopChop, UCSC genome brower

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    Possibly use NCBI databse to find genome sequences. pyhton program to perform genome assembly a 3-4 pages documents describing 1. data collection and method 3. results evaluation It'll be great if you know how to use bioinfo databases like ChopChop, UCSB genome brower

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    I need a Java program to do a blast search on a DNA sequence (such as any record in this file) against the NCBI nucleotide database. The EBI has a client interface for doing Blast search against NCBI database See the attached for more

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    Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS-FTD-linked UBQLN2 mutations. - PubMed - NCBI. Not writing some explanation ( detailed and figures )

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    Hi, Get FASTA sequences from BLAST tool (automate it) ( PROGRAM=blastp&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) for all the sequences compare the result with best match and save in db and show results . Thats all

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    Hi, Get FASTA sequences from BLAST tool (automate it) ( PROGRAM=blastp&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) for all the sequences compare the result with best match and save in db and show results . Thats all

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    Hi, Get FASTA sequences from BLAST tool (automate it) ( PROGRAM=blastp&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) for all the sequences compare the result with best match and save in db and show results . Thats all

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    Hi, Get FASTA sequences from BLAST tool (automate it) ( PROGRAM=blastp&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) for all the sequences compare the result with best match and save in db and show results . Thats all

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    Hi, Get FASTA sequences from BLAST tool (automate it) ( PROGRAM=blastp&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) for all the sequences compare the result with best match and save in db and show results . Thats all

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    Hi, Get FASTA sequences from BLAST tool (automate it) ( PROGRAM=blastp&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome) for all the sequences compare the result with best match and save in db and show results . Thats all

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    i want complete web application with script in java or python by using biojava or biopython in which biological formats convert into other option file upload and copy paste in input time and output time download option an...files include script must include different functions for all formats links i want this formats.. Input formats and Available output formats are listed below. Fasta :converted into pir,phylip,genbank,seqxml. Fastq: converted into fasta, pir, genbank, phylip, qual. PIR :converted into fasta, phylip, genbank, seqxml. Phylip: converted into fasta, genbank, pir. PDB: converted into fasta,pir,phylip and genbank GenBank: converted into fasta, phylip, pir, seqxml. Seqxml Qual: converted into fasta and fastq

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    Copy some journal article PMIDs from NCBI based on journal name. Following is an example query link:

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    ...need the following python scripts: Script #1: Convert into by extracting the "Organism name" and the "Sequence" values from into Sample.fasta. The should look like this: > Organism_name 1 Sequence 1 > Organism_name 2 Sequence 2 ... (pay attention that in , the "Organism Name" column contains two words that are separated by space. In the .fasta file, I need to replace this space with an underscore: e.g. "Escherichia coli" from should be converted into "Escherichia_coli" in ). Script #2: Extract lines from and write them into several .csv files by using keywords from file. For example: if the contains the following values: TACK Asgard Microarchaeota then

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    Looking for someone who is proficient in Bioinformatics tools such as NCBI, Blast, Clustal, MAFFT, Muscle, and T-Coffee. I've attached the assignment. It is short so I expect an expert to complete it quickly. There is a weekly assignment like this for the upcoming 3 weeks.

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    ...scientific backing. Our goal is for consumers to gain valuable, actionable information about genetic tests, how they work, and how the industry is involving. Educating the lay audience is a major objective. The ideal candidate has knowledge of and ability to clearly communicate biology/genetics concepts to a lay audience. We may occasionally ask you to summarize the findings of a research article from NCBI or PubMed, so experience with reading genomics field scientific papers and/or experience in a genomics lab is desired. Knowledge of the genetic testing industry is a plus. The time commitment is 5-10 hours/week, with the opportunity to adjust upward contingent upon performance. The candidate will mainly work with the marketing team to communicate on content strategy and objec...

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    Require 20 advantages of a certain vitamin supplement with well researched quotes and citations from medical journals. Looking for a Medical writer with experience to be who can also provide a TURNITIN REPORT. Research to be performed from NCBI website. English needs to be immaculate.

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    Task: Preprocessing high throughput sequencing data is an important step. One element of this is the removing of adapters and primers from sequenced reads. Your job is to design a program (in Pure Python) to parse a FASTA file, identify the forward and reverse primers, remove those regions (and any adapters) from those sequences, and create an output file of the trimmed reads. Furthermore, your program should create a second output file containing reads that were not trimmed and a log file of what happened during the trimming process.

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