Mac Installing R studio
0:46
Жыл бұрын
Mac Installing R and R tools
2:01
Mac Terminal
1:00
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Mac Security
0:51
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Logistic Regression
5:07
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Week Seven Workshop Chocolate
9:09
Height data ANOVA
9:38
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Cereals t tests
11:16
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Student Data t tests
5:03
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Stoats Island Evolution
13:58
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Week Seven Workshop Lateraility
7:39
Week 8 Cereals t test
4:42
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Week 8 Paired t Test
10:55
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Week 8 Periwinkles t Test
8:35
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Week 8 Significant Figures
9:16
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Week 8 Student Heights t test
4:33
Chi-squared Test for a 2x2 Table
7:00
Chi-squared Data Analysis in SPSS
5:46
Transformed Regression in SPSS
14:41
Regression in SPSS
36:00
Жыл бұрын
Starting the Literature Review
29:44
2 жыл бұрын
Пікірлер
@shygardener3290
@shygardener3290 Ай бұрын
Hello. I would like to ask how you created the Muscle/FastTree Shell was created.
@justinlloyd8441
@justinlloyd8441 2 ай бұрын
Hi Andrew. I keep getting this error: "Exception: Cannot invoke "String.trim()" because "<local1>" is null". Any advice on what it means?
@MostDeviantAsiedu
@MostDeviantAsiedu 3 ай бұрын
How did you calculate the effect size
@aljanespinas503
@aljanespinas503 3 ай бұрын
How to redo in fig tree?
@jadehamilton5959
@jadehamilton5959 4 ай бұрын
Hi Andrew, I have an aligned cytochrome b sequence from MEGA to input into BEAUTI to find out the time of divergence. I am using a mutation rate of 0.159. How can I estimate time in BEAUTI and then BEAST? Its all very complicated. Much help will be appreciated.
@aditisingh3986
@aditisingh3986 9 ай бұрын
hey, can you please send the data to plot inward funnel. I am not able to find it anywhere. It is urgent thank you
@rociogerez5802
@rociogerez5802 9 ай бұрын
I am having troubles accessing to the Epiflu information, It works for epicov, epipox and epiarbo, but not for flu. Am I doing something wrong?
@zmkhan8610
@zmkhan8610 10 ай бұрын
Hello there i am begginer and trying to learn new stuff from where did i get the first page what is its name we should search on google to download protein
@vovoghurejhor8784
@vovoghurejhor8784 10 ай бұрын
ncbi
@anindyabiswas1831
@anindyabiswas1831 11 ай бұрын
Life-saving. Keep up the good work🎉
@ElisKhatizah
@ElisKhatizah 11 ай бұрын
Hi, do you know how to open the 'epiFlu' window? I have tried so many times but there was no change in my GISAID window. I only can access epiCov, epiPox, and epiArbo after registration.
@TheJanbal
@TheJanbal Жыл бұрын
Can you kindly let me know how to do meta analysis on prevalence studies
@kharismaajimartadi1719
@kharismaajimartadi1719 Жыл бұрын
hi sir can you tell us what the version of spss is this?
@psjmartinez
@psjmartinez Жыл бұрын
Is it possible to do a meta-analysis of cross-sectional studies?
@afokekokogho5477
@afokekokogho5477 Жыл бұрын
If you do a large study & u see a high significance, u are more likely to report it. Correct that. Must be a slip of tongue
@andrewdalbyUW
@andrewdalbyUW Жыл бұрын
With large studies you are going to see more significance but a smaller effect size. You see more significance because the standard error of the mean is smaller BUT the effect size is less likely to be a biased estimate and it is most likely to be smaller.
@NurArshad
@NurArshad Жыл бұрын
Hii. May I know if the registration takes a long time to be process?? Need to be able to access to retrieve the sequences for my project but still haven’t got the access 🥺
@emmanuelisaac2217
@emmanuelisaac2217 Жыл бұрын
Link to download the file??
@gogomyu9513
@gogomyu9513 Жыл бұрын
hey, really helpful video! can you help me more? how can i mix two fasta files and use an output then in a new file?
@sihabyoutube
@sihabyoutube Жыл бұрын
kzbin.info/door/QvmTWPNks387TJKZ8WXktA
@grigory-2336
@grigory-2336 Жыл бұрын
How can I the sps macro for the meta analysis to the SPSS? I want to add Wilson macro
@fernandojaramillo1543
@fernandojaramillo1543 Жыл бұрын
Great video. Can you also run correlation based meta-analyses in SPSS?
@yusun9608
@yusun9608 Жыл бұрын
if I have some partitioned, how to add the prior? for every trees?
@augustodirham853
@augustodirham853 Жыл бұрын
Thank you for this video. I have align a large dataset (too large for the EMBL Clustal-O server). I hope a local install will help.
@bestudious6212
@bestudious6212 Жыл бұрын
Heyyyy plz help me
@Loweezy82898
@Loweezy82898 2 жыл бұрын
When you are customizing the fasta headers for download, you can delete all of the default information and then add your fasta headers in the order you would like them to appear in your final output. I agree, all of the fields I would like are not present, but if host is what you want, you can download the fasta with the strain name and parse out the host, if that is important.
@gladysomonikobe4145
@gladysomonikobe4145 2 жыл бұрын
Thanks
@tonyjehi3951
@tonyjehi3951 2 жыл бұрын
Which version of SPSS is this?
@ericreinbold5026
@ericreinbold5026 2 жыл бұрын
Is this Grad Pack Premium or the Faculty Version?
@andrewdalbyUW
@andrewdalbyUW 2 жыл бұрын
The faculty version
@user-mh5qw2su1l
@user-mh5qw2su1l 2 жыл бұрын
sir can I ask which what kind of data I need to include in my raw data (like Cronbach’s alphas R-squareds ), can u name all help to answer the factors that should be included in the raw data ?
@comedychannel6012
@comedychannel6012 2 жыл бұрын
Dear Sir, thank you so much for your video. Could I draw the picture with Funnel Plot in this software?
@tantrilestari4897
@tantrilestari4897 2 жыл бұрын
Hi, My Name is Tantri. currently, I'm trying to download clustal omega but don't know why I cannot access to their website. do you know why?
@ameersohailsyed6243
@ameersohailsyed6243 2 жыл бұрын
one of the best lecture heard very practical and clear
@godspeed8045
@godspeed8045 2 жыл бұрын
Can you make one video for dichotomous variable
@user-cg2kk2uo9e
@user-cg2kk2uo9e 2 жыл бұрын
Can you please upload that making phylogenetic tree including ‘sequence’ and ‘year’ at the same time.
@gypsyrose4821
@gypsyrose4821 2 жыл бұрын
HELP!!!!
@barbarapiecek9194
@barbarapiecek9194 2 жыл бұрын
your videos are very good and have a wide message thank you
@user-wi9zl5ur8o
@user-wi9zl5ur8o 2 жыл бұрын
Dear Sir Andrew, appreciate your tutorial instruction. Could I require to raise a question? I have a problem with OMA. I can not save the data after running the process. The running results can be saved but the data in the form can not be saved in OMA form. How should I solve the problem? Thank you very much.
@raniaseddaoui3248
@raniaseddaoui3248 2 жыл бұрын
Do I have to register on the database so that I can extract the sequences ? If so , please tell me how ?
@raniaseddaoui3248
@raniaseddaoui3248 2 жыл бұрын
Do I have to register on the database so that I can extract the sequences ? If so , please tell me how ?
@raniaseddaoui3248
@raniaseddaoui3248 2 жыл бұрын
Do I have to register on the database so that I can extract the sequences ? If so , please tell me how ?
@shaahyna
@shaahyna 2 жыл бұрын
Amazing! Thank you so much :)
@Ilemaurice687
@Ilemaurice687 2 жыл бұрын
Any mail to contact you ?
@temitopeibrahimamosa2885
@temitopeibrahimamosa2885 2 жыл бұрын
I do meta-analysis at low price
@Ilemaurice687
@Ilemaurice687 2 жыл бұрын
@@temitopeibrahimamosa2885 i have my mail on my description channel
@andrewdalbyUW
@andrewdalbyUW 2 жыл бұрын
@Ilemaurice687
@Ilemaurice687 2 жыл бұрын
Hello Sir i got a question i dont know how to do it can i sent it to you if possible please
@nomansadiq5929
@nomansadiq5929 2 жыл бұрын
Thank you so much made life easy can you tell the version of SPSS ?
@andrewdalbyUW
@andrewdalbyUW 2 жыл бұрын
This is version 28
@OsvaldoLaurindo
@OsvaldoLaurindo 2 жыл бұрын
Please help me, I am trying to do a multiple alignment of HA Flu sequences using Muscle but keeps getting an error "Stop codon(s) are found in the translated sequences. Please select a correct Genetic Code or coding frame."
@andrewdalbyUW
@andrewdalbyUW 2 жыл бұрын
Dear Osvaldo, You have the gene segments and not the coding segments. If you have the gene segments then you can have some regions before the start codon and so there are issues with the reading frame. You can solve this by either downloading the coding sequences or by doing a DNA alignment and ignoring the stop codon error. You cannot do a codon alignment until you have cut off all the sequence before the start codons.
@OsvaldoLaurindo
@OsvaldoLaurindo 2 жыл бұрын
@@andrewdalbyUW Thank you so much, problem solved.
@TheGriu
@TheGriu 2 жыл бұрын
Thanks! Amazing explanation!
@AlunaScape
@AlunaScape 2 жыл бұрын
Thank you for the info, but I've one question: If I want to download a bulk of filtered sequences of SARS-CoV-2 via gisaid, how can I do it?
@emilymiguel8198
@emilymiguel8198 2 жыл бұрын
Thank you! You saved me, I was getting so frustrated.
@andrewdalbyUW
@andrewdalbyUW 2 жыл бұрын
Glad it helped
@thomasjamonneau514
@thomasjamonneau514 2 жыл бұрын
You should not put 20% burn in without asking yourself other questions, as, if theses 20% are really not convergent with the rest of my data, meaning they aren't at the equilibrium. Most of the time, you have already use a burn in tool as with Log Combiner. At this state, you should avoid to sacrifice this much data, and put lower values of burn in to keep more of the variability from your data set. I hope this is clear ^^
@oldnewgaming9447
@oldnewgaming9447 2 жыл бұрын
Thanks alot
@andrewdalbyUW
@andrewdalbyUW 2 жыл бұрын
Most welcome
@aryasorensen4028
@aryasorensen4028 2 жыл бұрын
kzbin.info/www/bejne/o3bPXn1rZtiMi7c